Aventis Pasteur Bayer BioPort Cargill Turkey Products Chiron Behring Coca-Cola ConAgra Foods Frito-Lay Glaxo Wellcome Jade Pharmacy Kellogg Lederle Laboratories North American Vaccine Novartis Consumer Health Procter & Gamble Roche SmithKline Beecham Unilever Wegmans Food Markets Wilson Foods Company ActHIB Certiva Coca-Cola Classic Contac Dexatrim  Diet Coke Dr. Pepper Eskornade Fruitopia Strawberry  Passion Fresca Soda Pop  Havrix Infanrix IPOL Lay's Classic Potato Chips  Lotronex Minute Maid Nestea Iced Tea OmniHIB PNU-IMUNE23 Powerade StarLink  Trasylol Triaminic alosetron aspartam bromiany Cry9C protein drożdże Escherichia coli O157H7 FD&C Yellow No. 5. fenylpropanolamina  fragmenty uszczelki guarana extract kawałki szkła  kwas arystolochowy Listeria monocytogenes pleśnie transgeniczna kukurydza  ukryta laktoza ukryta pszenica ukryte migdały ukryte orzechy ziemne ukryte składniki mleczne ukryty acesulfam K ukryty cukier ukryty sód ukryty sztuczny barwnik żywność funkcjonalna

    Część
    III
    Firmy
    (kolejność alfabetyczna)
    Markowe produkty
    (kolejność alfabetyczna)
    Zagrożenia zdrowia
    (kolejność alfabetyczna)
    Aventis Pasteur
    Bayer
    BioPort
    Cargill Turkey Products
    Chiron Behring
    Coca-Cola
    ConAgra Foods
    Frito-Lay
    Glaxo Wellcome
    Jade Pharmacy
    Kellogg
    Lederle Laboratories
    North American Vaccine
    Novartis Consumer Health
    Procter & Gamble
    Roche
    SmithKline Beecham
    Unilever
    Wegmans Food Markets
    Wilson Foods Company
    ActHIB
    Certiva
    Coca-Cola Classic
    Contac
    Dexatrim 
    Diet Coke
    Dr. Pepper
    Eskornade
    Fruitopia Strawberry Passion
    Fresca Soda Pop
     Havrix
    Infanrix
    IPOL
    Lay's Classic Potato Chips
    Lotronex
    Minute Maid
    Nestea Iced Tea
    OmniHIB
    PNU-IMUNE23
    Powerade
    StarLink 
    Trasylol
    Triaminic
    alosetron
    aspartam
    bromiany
    Cry9C protein 
    drożdże
    Escherichia coli O157H7
    FD&C Yellow No. 5.
    fenylpropanolamina 
    fragmenty uszczelki
    guarana extract
    kawałki szkła 
    kwas arystolochowy
    Listeria monocytogenes
    pleśnie
    transgeniczna kukurydza 
    zatajona farba
    zatajona laktoza
    zatajona pszenica
    zatajone migdały
    zatajone orzechy ziemne
    zatajone składniki mleczne
    zatajony acesulfam K
    zatajonycukier
    zatajony sód
    żywność "funkcjonalna"


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    Pseudomonas sp. w kosmetykach firmy Soroko Inc.

    (jakość i skład kosmetyków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE KOSMETYKÓW)
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    February 9, 2001
    Soroko Facial Spray Recalled for Contamination

    Clifton, NJ (SafetyAlerts) -  . said today it is recalling Rejuvenating Mist facial spray because the product may be contaminated with Pseudomonas sp.

    Soroko has not received any reports of illness to date.

    The product has a green label that says "Soroko, Inc." and identifies Blade Laboratories of Ontario, Canada as the manufacturer.

    According to a company press release the product was distributed mainly in New York, New Jersey, Texas, Mexico, Scotland, and Canada.

    In January, laboratory tests showed that samples of the spray were contaminated with pseudomonas, bacteria that can cause serious infection in humans, particularly if it gets into open wounds. If introduced into the eyes, such as from a facial spray, pseudomonas can cause vision-damaging infection.

    Consumers should discard the product immediately or return it to where it was purchased. Consumers with questions can call the company at 1-973-472-6501 between 9 a.m. and 4 p.m. EST Monday through Saturday.


    Listeria monocytogenes w produktach drobiowych firmy Serenade Foods, Inc.
    (Bakterie w polskich produktach:
    ZANIECZYSZCZENIA MIKROBIOLOGICZNE
    LIMITOWANE W ŚRODKACH SPOŻYWCZYCH)
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    February 10, 2001
    Serenade Foods (Maple Leaf Farms) Recalls 6,000 lbs. of Duckling Products

    Milford, IN (SafetyAlerts) - Serenade Foods, Inc.   also doing business as Maple Leaf Farms, has announced a voluntary recall of approximately 6,000 pounds of duckling products that may be contaminated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service has  announced.

    The duckling products were produced on Jan. 10, and distributed to food service establishments in California, Florida, Illinois, Massachusetts, Michigan, New York, Nevada, North Carolina, Pennsylvania, Texas, and Wisconsin.

    Food service products subject to recall include:

    "SYSCO IMPERIAL PARTIALLY BONED FULLY COOKED ROASTED YOUNG DUCKLING HALVES" in 8.25 lb. boxes with a package code of 011001; and
    "Maple Leaf Farms PARTIALLY BONED ROASTED YOUNG DUCKLING HALVES"in 7.5 lb. boxes with a package code of 1010;
    All products being recalled bear the establishment number "EST. P-2375" inside the USDA seal of inspection.

    "Because of the potential for foodborne illness, we want consumers to be aware of the recall," said Tom Billy, FSIS administrator. "Purchasers or consumers of duckling may wish to ask restaurants or places where they consume duckling if the product or meal contains the recalled product."

    The company notified FSIS of a positive Listeria monocytogenes test result and initiated a recall.

    This is the second voluntary product recall by Serenade Foods, Inc., this year. On Jan. 16, the company recalled 4,400 pounds of duckling product for possible Listeria monocytogenes contamination.

    Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. Listeriosis can cause high fever, severe headache, neck stiffness, and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weak immune systems--infants, the frail or elderly, and persons with chronic disease, with HIV infection, or taking chemotherapy.

    FSIS has received no reports of illness associated with consumption of this product. Anyone concerned about an illness should contact a physician.

    Consumers and media with questions about the recall may contact Dan Harper, Serenade Foods Corporate Communications Manager at (219) 658-4121.

    Consumers with food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time) Monday through Friday, and recorded food safety messages are available 24 hours a day.


    Wytworzone w antysanitarnych warunkach produkty firmy Coca Cola Bottling Co.
    (wymagania sanitarne dla polskich produktów:
    POLSKIE PRZEPISY SANITARNE DOTYCZĄCE WODY
    POLSKIE PRZEPISY SANITARNE
    DOTYCZĄCE ARTYKUŁÓW SPOŻYWCZYCH)
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    February 14, 2001
    FDA First Notice: Coke Recalls 2 Liter Bottles

    Jacksonville, FL (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Coca Cola Bottling Co. is recalling - or has recalled - Coca-Cola Classic, 2 liter plastic bottles because the product was manufactured under unsanitary conditions whereby it may have become contaminated with filth.

    This is the first public notice of this Class III recall issued by FDA.

    PRODUCT
    Coca-Cola Classic, 2 liter plastic bottles.

    Recall #F-207-1.

    CODE:
    JAN2201JAA, JAN2202JAD and JAN2201JAE.

    MANUFACTURER:
    Coca Cola Bottling Co., Jacksonville Plant aka Coca-Cola Enterprises Bottler, Jacksonville, FL.

    RECALLED BY:
    Manufacturer by faxed memo on 10/30/00. Firm-initiated recall *complete.

    *Completed recall: FDA states 'completed recall' indicates the company has removed all affected product from store shelves,  it does not necessarily mean this particular product lot, or codes, have been fully accounted for.

    DISTRIBUTION:
    Florida and Georgia.

    QUANTITY:
    25,190 cases, 12 per case.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


    Pestycyd Aldicarb w produktach drobiowych firmy Gold Kist Inc.
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    February 15, 2001
    420,000 lbs. of Chicken Recalled

    Sumter, SC (SafetyAlerts) - Gold Kist Inc. is voluntarily recalling approximately 421,000 pounds of chicken products that may be contaminated with the pesticide Aldicarb, the U.S. Department of Agriculture’s Food Safety and Inspection Service announced today.

    Gold Kist Inc. notified FSIS of the possible contamination. The products subject to recall were sent to distributors and retail establishments nationwide. Products were produced on January 29 and are marked with the establishment number "P-17980" inside the USDA seal of inspection.

    Products subject to recall are:
    Gold Kist Farms premium fresh "SPICY HOT FRYING CHICKEN WING PORTIONS," with package code "406000."

    Gold Kist Farms "YOUNG CHICKEN FRONT HALF SHELLS WITH ATTACHED SKIN AND NECK," with package code "170048."

    Gold Kist Farms "FRYING CHICKEN PARTS JUMBO WHOLE LEGS with skin and fat attached," with package code "70008."

    10 lb. bags of Gold Kist Farms "BONELESS, SKINLESS CHICKEN BREAST MEAT WITH RIB MEAT," with package code "230050."

    Gold Kist Farms "FRYING CHICKEN TENDERLOINS Big Bird," with package code "460010."

    Gold Kist Farms "FRYING CHICKEN PARTS BONELESS, SKINLESS WHOLE LEG MEAT," with package code "450000."

    Gold Kist Farms "BIG BIRD FRYING CHICKEN PARTS WHOLE WINGS," with package code "350021."

    2.5 lb. bags of Gold Kist Farms "BONELESS SKINLESS CHICKEN BREASTS," with package code "8420."

    4 lb. bags of Gold Kist Farms "SEPARATED CHICKEN WINGS," with package code "8464."

    Gold Kist Farms "GRANDY’S MARINATED CHICKEN BREAST FILLETS WITH RIB MEAT," with package code "7108."

    Gold Kist Farms "SOUTHERN STYLE CHICKEN TENDER FRITTERS," with package code "8272," "7272," or "7072."

    Gold Kist Farms "BREADED CHICKEN GIZZARDS," with package code "7501."

    Gold Kist Farms "DICED WHITE YOUNG CHICKEN MEAT," with package code "279."

    Gold Kist Farms "BLAZING WINGS CHICKEN WING SECTIONS," with package code "8086."

    Gold Kist Farms "CHICKEN WING SECTIONS," with package code "8076."

    WAL-MART SUPERCENTER, "HOT’ N SPICY BREAST STRIPS- Chicken Breast Strip Fritters," with package code "40021" and item number "8009908."

    WAL-MART SUPERCENTER "ORIGINAL BREAST STRIPS- Chicken Breast Strip Fritters," with package code "40020" and item number "8009943."

    "CN- ROASTED CHICKEN PATTIES," with package code "6620."

    "We urge consumers to check their refrigerators and freezers," said Margaret O’K. Glavin, acting FSIS administrator. "If they find any of the products listed above, consumers should not eat them, but return them to the point of purchase."

    At high concentrations, Aldicarb can cause weakness, headache, nausea, vomiting, and seizures. FSIS has received no reports of illnesses associated with consumption of this product. Anyone concerned about an illness should contact a physician.

    Consumers and media with questions about the recall may contact Paul Brower, vice president of corporate relations, Gold Kist Inc., at (770) 393-5312.

    Consumers with other food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time), Monday through Friday, and recorded food safety messages are available 24 hours a day.


    Zatajone orzechy ziemne w produktach firmy Great Skott Foods
    (NIEPOŻĄDANE REAKCJE NA PRODUKTY SPOŻYWCZE)
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    February 16, 2001
    Allergy Alert:  Great Skott Foods Recalls Yogurt Raisins for Undeclared Peanuts

    Milwaukee, WI (SafetyAlerts) - Great Skott Foods has announced it is recalling its 16 oz. Yogurt Raisins packed under the Great Skott label (bar-code #74526 70177), because it may contain undeclared peanut pieces.

    No illnesses have been reported to date.

    These Yogurt Raisins are 16 oz. and come in a clear cellophane bag. The problem bags come with a 0201 or 0202 code in the lower right hand corner of the white rear label under the nutritional information and were distributed to grocery stores in Wisconsin.

    People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.

    The recall was initiated after the U.S. Food and Drug Administration in response to a consumer complaint found that the yogurt raisins contained yogurt peanuts and peanut pieces.

    Consumers who have purchased Great Skott Foods (Yogurt Raisins) with the above codes are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Great Skott Foods at 414-291-9977.


    Niepoddane dostatecznej obróbce cieplnej produkty drobiowe firmy Tyson Foods, Inc.

    (POLSKIE PRZEPISY SANITARNE
    DOTYCZĄCE ARTYKUŁÓW SPOŻYWCZYCH)
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    February 20, 2001
    Tyson Foods Recalls 2.3 Million Pounds of Chicken

    Rogers, AR (SafetyAlerts) - Chick’n Quick, a Tyson Foods, Inc. plant, has announced a voluntary recall  affecting approximately 2.3 million pounds of cooked chicken because the products may have been underprocessed.

    All products being recalled were produced between Dec. 19, 2000 and Feb. 16, 2001 and bear the establishment number "P-7221" inside the USDA seal of inspection on the label. Additionally, all products bear a UPC number as indicated below and a production code with a Julian calendar date as the first four digits of the number. The production codes range from 3540 through 3660 (Dec. 19, 2000 through Dec. 31, 2000) and 0011 through 0471 (Jan. 1, 2001 through Feb. 16, 2001).

    The products were distributed to retail establishments, restaurants, and food service establishments nationwide and in Bermuda, Bahrain, Cayman Islands, Guyana, Indonesia, Panama, Puerto Rico, Saudi Arabia, and St. Martin. Products were also distributed to military installations nationwide and abroad.

    The following products subject to recall were distributed to retail establishments:
     
     

       
       
      Product Description UPC Number
      Tyson Spicy Breast Tenderloins, Breaded Chicken Breast Tenderloins 23700-02183
      Tyson Breast Fillets, Breaded Chicken 23700-02360
      Tyson Breast Tenderloins, Breaded Chicken Breast Tenderloins 23700-02360
      Tyson Southern Fried Breast Fillets, Breaded Chicken 23700-02362
      Tyson Southern Style Breast Tenderloins 23700-02362
      Tyson Buffalo Style Chicken Strips 23700-03802
      Tyson Crispy Chicken Strips 23700-03803
      KIRKWOOD Breaded Chicken Southern Style Breast Fillets 41498-18026
      Schwan's Southern Style Chicken Breast Tenderloin Strips 000-23700-56237
      Food Club Chicken Breast Fillets 36800-77177
      MEIJER Breaded Chicken Breast Fillets 41250-96432
      HILL COUNTRY FARE CHICKEN BREAST TENDERLOINS 41220-21735
      Shaws CHICKEN BREAST FILLETS 45674-58013
      Weis BREADED Chicken BREAST TENDERLOINS 41497-04635
      HyVee Chicken Breast Fillets 75450-15050
      Great Value FRITTER STYLE Breast Tenderloins 78742-37346
    The following products subject to recall were distributed to restaurants, food service establishments, and military installations:
     
       
       
      Product Description Product Number UPC Number
      Breaded Chicken Breast Tenderloins 2584-895 000-74865-08472
      Breaded Chicken Breast Tenderloins 2584-928 000-23700-31324
      Chicken Breast Strip Fritters 3803-861 000-23700-51771
      Buffalo Bites 5474-633 000-23700-52525
      FC Breaded Chicken Breast Fillets (100% Tenderloins) 30299-525 000-11621-30299
    "Because of the potential for foodborne illness, we urge consumers to check their refrigerators and freezers to see if they have purchased any of these cooked products," said Margaret O’K. Glavin, Associate Administrator of the USDA's Food Safety Inspection Service (FSIS). "If they find the recalled products, consumers should not eat them, but return them to the point of purchase. Purchasers or consumers of chicken may also wish to ask restaurants or places where they consume chicken if the meal contains the recalled products."

    The problem was discovered through Tyson’s Quality Assurance program based on consumer complaints. The establishment then notified FSIS. No illnesses associated with consumption of the product have been reported to FSIS. Anyone concerned about an illness should contact a physician immediately.

    Consumers with questions about the recall may contact Willie Barber, Tyson’s Manager of Consumer Relations Department at (501) 290-4714.

    Media with questions about the recall may contact Ed Nicholson, Tyson’s Director of Media and Community Relations, at (501) 290-4591.

    Consumers with food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time), Monday through Friday, and recorded information is available 24 hours a day.


    Zatajone farby w produktach firmy Gourmet Foods International

    (dawki E 102 i E 110 w polskich produktach:
    BARWNIKI ŻYWNOŚCI I NAPOJÓW)
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    February 21, 2001
    Gourmet Foods International Recalls Egg Rolls

    Nashville, TN (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Gourmet Foods International is recalling five of its Oriental Delight brand frozen egg roll products as described below,  because the products contain undeclared FD&C Yellow No. 5 and FD&C Yellow No. 6.

    This is the first public notice of this Class II recall issued by FDA.

    PRODUCT
    Oriental Delight brand frozen egg rolls:
     

  1. F-233-1 Shrimp and Pork Egg Rolls 60/3oz/carton (item no. 100603) and 100/2oz/carton (item no.) 102100
  2. F-234-1 Shrimp Egg Rolls 60/3oz/carton (item no. 200603)
  3. F-235-1 Vegetable Egg Rolls 60/3oz/carton (item no. 300603)
  4. F-236-1 Petite Shrimp Egg Rolls 200/0.5oz/carton (item no. 205200)
  5. F-237-1 Petite Vegetable Egg Rolls 200/0.5oz/carton (item no. 305200)

  6. CODE:
    Any and all Lot Numbers with the following product codes: 100603,200603, 300603, 102100, 205200, and
    305200.  The firm maintains that a six digit ink stamp code is supposed to be appled to each carton. This may/may not be done, and if done, the six digit code may be a pack date, a ship date, or a getting ready to ship date.

    MANUFACTURER:
    Gourmet Foods International, Nashville, TN.

    RECALLED BY:
    Manufacturer, by FAX on 12/22/00. FDA-initiated recall ongoing.

    DISTRIBUTION:
    Charlotte, NC and Lexington, SC.

    QUANTITY:
    460 cases of the various products.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.
     


    Zatajone farby w produktach firmy Tortilla King, Inc.

    (dawki E 102, E 110 i E 129 w polskich produktach:
    BARWNIKI ŻYWNOŚCI I NAPOJÓW)
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    do bezpieczeństwa i odszkodowania za uszkodzenie ciała lub rozstrój zdrowia
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    February 21, 2001
    FDA First Notice: Tortilla King Recalls Certain Corn Tortillas

    Moundridge, KS (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Tortilla King, Inc.  is  recalling - or has recalled - certain lots of its Mama Lupe's Fresh Corn Tortillas because the product contains undeclared FD&C Yellow No. 5, FD&C Yellow No. 6 and FD&C Red No. 40.

    This is the first public notice of this Class II recall issued by FDA.

    PRODUCT
    Mama Lupe's Fresh Corn Tortillas in 25-oz. packages, 24 corn tortillas per package, 24 packages per case.
    The responsible firm on the label is Tortilla King, Inc., Moundridge, KS.

    Recall #F-245-1.

    CODE:
    Expiration date JAN 22 or earlier.

    MANUFACTURER:
    Tortilla King, Inc., Moundridge, KS.

    RECALLED BY:
    Manufacturer, via telephone on 1/3/01. FDA Initiated recall *complete.

    *Completed recall: FDA states 'completed recall' indicates the company has removed all affected product from store shelves,  it does not necessarily mean this particular product lot, or codes, have been fully accounted for.

    DISTRIBUTION:
    KS, OK, and MO.

    QUANTITY:
    Approximately 300 /24-count cases.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.
     


    Zatajone farby w produktach firmy Petri Baking Products, Inc.

    (dawki E 102 i E 110 w polskich produktach:
    BARWNIKI ŻYWNOŚCI I NAPOJÓW)
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    do bezpieczeństwa i odszkodowania za uszkodzenie ciała lub rozstrój zdrowia
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    FDA First Notice: Petri Baking Products Recalls Certain Lots of its Bakery Fresh Lemon Cookies
    February 21, 2001

    Silver Creek, NY (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Petri Baking Products, Inc. is  recalling certain lots of its Bakery Fresh Lemon Cookies because the product contains undeclared FD&C Yellow No. 5 and FD&C Yellow No. 6.

    This is the first public notice of this Class II recall issued by FDA.

    PRODUCT
    Bakery Fresh Lemon Cookies, Net Wt 8.9 oz (252 g) Responsible firm on the label: Distributed by Petri Baking Products Silver Creek.

    Recall #F-248-1.

    CODE:
    Lot numbers are as follows: 00760, 00390, 10110, 12020, 01260, 01490, 11210, 12720, 02660, 02090, 11510, 02911, 01770, 02790, 12910, 01311, 00180, 10800, 10520, 02121, 02780, 12200, 11020
    Code breakdown: 1st & 4th digit = month 2nd & 3rd digit = day 5th digit = year.

    MANUFACTURER:
    Petri Baking Products, Inc., Silver Creek, NY.

    RECALLED BY:
    Manufacturer, by letters dated 9/26/00 and 11/13/00. This ongoing recall was initiated and audited by the New York State Dept. of Agriculture & Markets.

    DISTRIBUTION
    IL, KS, MA, MD, MI, MS, NH, NJ, NY, OH, PA, and WV.

    QUANTITY:
    6,681 cases x 18 units per case.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


    Cuchnąca olejem napędowym niskokaloryczna coca-cola
    powoduje zachorowanie na Harwardzie

    (zatrucia produktami firmy Coca-Cola w 1999r.:
    CZARNA LISTA STOWARZYSZENIA
    OCHRONY ZDROWIA KONSUMENTÓW)
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    February 22, 2001
    Diet Coke has a smell similar to diesel fuel and makes a member of the Harvard Community ill

    Harvard University Police

    Community Advisory
    This notice is part of the Department's ongoing efforts to provide community awareness.

    Safety Advisory

    On Thursday February 22, 2001, a member of the Harvard Community purchased a 20-ounce bottle of  Diet Coke that contained a foreign substance that made the person briefly ill.   The bottle was purchased from a vending machine in Loker Commons.  At this time, we do not know if there are any other instances of contaminated bottled beverages on campus.

    Initial reports are that the Diet Coke had a smell similar to diesel fuel, but the exact nature of the foreign substance has not yet been determined and is being investigated.

    The University would like the Harvard Community to be aware of this incident.  Consumers should inspect similar bottled beverages before consuming them and report any unusual contents to HUPD.

    Anyone with any knowledge of this incident or who becomes aware of information regarding this or similar incidents is encouraged to contact the Harvard University Police Department at 617-495-1212.

    Susan Zawalich
    Dudley House Administrator
    Harvard University
    Lehman Hall, 3rd Floor
    (617) 495-2255
    FAX: (617) 496-5459


    Cuchnące olejem smarowniczym produkty firmy Kraft Foods

    (POLSKIE PRZEPISY SANITARNE
    DOTYCZĄCE ARTYKUŁÓW SPOŻYWCZYCH)
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    February 28, 2001
    Kraft Foods Recalls Easy Mac

    Rye Brook, NY (SafetyAlerts) - Kraft Foods is recalling certain code dates of its Kraft Easy Mac microwaveable macaroni and cheese dinner. The product may have an off-flavor or off-odor caused by contact with food-grade lubricating oil due to an equipment failure.

    Kathy Knuth, a spokesperson for Kraft, was quick to point out that there is no health or safety risk with the recalled product, but some people may have a greater sensitivity to the off flavor or odor. The company is working with the Food and Drug Administration (FDA) regarding the issue.

    The product was distributed in the United States, and no other varieties of Kraft macaroni and cheese dinner are part of the recall..

    This recall was initiated on February 6, 2001.  FDA had not yet classified this recall when contacted this afternoon.

    Product codes being recalled are: SEP-05-01 through SEP-26-01.

    The company stated that most of the product had been recovered prior to reaching consumers, however could not specify how much product was involved in the recall.

    Consumers can return the product to their grocers for a full refund.  Consumers with questions should contact Kraft at (800) 847-1997, 9:00 a.m. - 5:00 p.m. Central Time, Monday through Friday.
     


    Niedostatecznie silnie działająca aspiryna firmy Leiner Health Products, Inc.

    (jakość i skład leków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    ŚRODKÓW FARMACEUTYCZNYCH
    I MATERIAŁÓW MEDYCZNYCH)
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    February 28, 2001
    (OTC) Adult Low Strength Enteric Coated Aspirin Recalled

    Carson, CA (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Leiner Health Products, Inc. is recalling certain lots of (OTC) Adult low strength enteric coated aspirin tablets because of superpotency.

    This is the first public notice of this Class III recall issued by FDA.

    PRODUCT
    (OTC) Adult low strength enteric coated aspirin tablets, 81 mg, 120 unit bottles.

    Recall #D-099-1.

    CODE:
    0032636; 0032637; 0032856; 0032858; 0033126; 0033127; 0033129; 0033203; 0033204; 0033459; 0043676; 0043691 and 0066784.

    MANUFACTURER:
    Time-Cap, Inc., Farmington, NY.

    RECALLED BY:
    Leiner Health Products, Inc., Carson, CA., by letter on 11/30/2000. Firm-initiated recall ongoing.

    DISTRIBUTION:
    MN, PA, NY, NC, MA, OH, CA, WA, CO, MD, AZ, OR, AR, FL.

    QUANTITY:
    109,716 bottles of 120 tablets each.


    Listeria monocytogenes w węgierskim salami

    (Bakterie w polskich produktach:
    ZANIECZYSZCZENIA MIKROBIOLOGICZNE
    LIMITOWANE W ŚRODKACH SPOŻYWCZYCH)
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    March 1, 2001
    3,700 lbs. of Salami Recalled in Seven States

    Saddle Brook, NJ (SafetyAlerts) - Liberty Richter is voluntarily recalling approximately 3,700 pounds of imported Hungarian salami that may be contaminated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service announced today.

    The product subject to recall is "PICK HUNGARIAN SALAMI" in 2.75 lb. sticks and bears the code "L23" on the label.

    The salami was produced in Hungary on Jan. 23, and distributed to retail establishments, including delis, in California, Illinois, Massachusetts, Michigan, New Jersey, New York, and Ohio.

    "Because of the potential for foodborne illness, we want consumers to be aware of the recall," said Thomas J. Billy, FSIS administrator. "Purchasers of salami packaged at the retail level may wish to ask if they received the recalled salami."

    FSIS discovered the problem through its routine import monitoring program for Listeria monocytogenes.

    Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. Listeriosis can cause high fever, severe headache, neck stiffness, and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weak immune systems--infants, the frail or elderly, and persons with chronic disease, with HIV infection, or taking chemotherapy.

    FSIS has received no reports of illness associated with consumption of this product. Anyone concerned about an illness should contact a physician.

    Consumers or media with questions about the recall may contact Kathie Gibbs Borkowski, Division Vice President of Operations at Liberty Richter, (201) 843-8900.

    Consumers with food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time) Monday through Friday, and recorded food safety messages are available 24 hours a day.
     


    Amoniak zamiast wybielacza chlorowego w środku czyszczącym firmy Super Valu

    (jakość i skład środków chemii gospodarczej w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    SUBSTANCJI I PREPARATÓW CHEMICZNYCH)
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    March 1, 2001
    Richfood Bleach Recalled by SuperValu Eastern Region

    Bleach recalledRichmond, VA (SafetyAlerts) - SuperValu Eastern Region is voluntarily recalling about 500 bottles of Richfood bleach. The bottles were mislabeled. The clear plastic 32 oz. bottles were labeled bleach, but contained ammonia. If the ammonia is mixed with bleach or acid, irritating or toxic gases could be produced.

    No injuries have been reported. This recall is being conducted to prevent the possibility of injury.

    The 32 oz. bottles of bleach were sold in supermarkets throughout Pennsylvania, New York, New Jersey, Maryland, and Northern Virginia from January 2001 through February 2001. The recalled bottles have a UPC Code of 11166 20961, which can be found on the back of the label, and sold for about $0.80. A warning on the back of the label says, "Do not use with toilet bowl cleansers, ammonia, or other household chemicals."

    Consumers should return the Richfood bottles of bleach to the store where purchased for a replacement or refund.

    For more information, call SuperValu toll-free at (866) 376-1257 between 9 a.m. until 5 p.m. ET Monday through Friday.


    Zagrażające życiu dzieci zabawki w restauracjach sieci McDonald's

    (bezpieczeństwo produktów w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    OGÓLNEGO BEZPIECZEŃSTWA PRODUKTÓW)
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    March 5, 2001
    McDonald's Recalls "Scooter Bug" Happy Meal Toys

    McDonald's Announce Recall of "Scooter Bug" Happy Meal ToysOakbrook, IL (SafetyAlerts) - McDonald's Corp. said today it is voluntarily recalling about 234,000 "Scooter Bug" toys. The toys were distributed with McDonald's Happy Meals for children under 3 years of age. The bug's antenna can break off, posing a choking hazard to young children.

    McDonald's has received two reports of children choking and one report of a child gagging on the broken off antenna.

    The Scooter Bug toy is about 3 inches long and 2 1/2 inch wide. When rolled across the floor, the bug's legs move back and forth. The bug has a yellow face with red antennas, orange feet and a purple body with green spots. The words "Fisher Price" are on the top of the toy. The words "MFG.FOR MCD CORP.CHINA" are on the rear of the toy.

    McDonald's restaurants in the U.S. and Canada distributed the toys with Happy Meals from November 2000 through February 2001.

    Parents should take the toy away from children immediately and return the toy to any McDonald's restaurant for a replacement toy. For more information, consumers should visit McDonald's web site at www.mcdonalds.com. Questions about this recall should be directed to CPSC's hotline at (800) 638-2772.


    Zatajony środek psychotropowy chlordiazepoksyd (elenium) w preparacie ziołowym
    Uwaga: po przyjęciu elenium nie wolno prowadzić pojazdów mechanicznych, spożywać alkoholu, wykonywać czynnosci wymagających niezbędnej koordynacji psychoruchowej, jak obsługa urządzeń, praca na wysokosci

    (jakość i skład leków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    ŚRODKÓW FARMACEUTYCZNYCH
    I MATERIAŁÓW MEDYCZNYCH)
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    March 7, 2001
    Anso Comfort™ Capsules Recalled

    Arcadia, CA (SafetyAlerts) - The Food and Drug Administration (FDA) has posted additional information concerning the Anso Comfort™ recall previously annouced by the California State Department of Health.   The product contains the undeclared prescription drug-chlordiazepoxide.

    This is recall has been classified Class II by FDA.

    PRODUCT
    (OTC) Anso Comfort™ Capsules, Extract of Hainanensis Merr Leaf, 200 mg, 60 capsules per bottle.

    Recall #D-100-1.

    CODE:
    Lot 0H0041, Sept 2003 and Lot 9422, Exp 7-2002.

    MANUFACTURER:
    Numeridian, Inc., Arcadia, CA.

    RECALLED BY:
    Manufacturer, by letter on 2/5/01. Firm-initiated recall ongoing.

    DISTRIBUTION:
    AK, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, PA, RI, SC, TN, TX, UT, VA, WA, and WI.
    Foreign distribution was to China (Shanghai), and Canada (BC and Ontario).

    QUANTITY:
    Lot OH0041, 6420 bottles; Lot 9422, unknown.
     


    Zagrażające życiu dzieci zabawki w restauracjach sieci Burger King

    (bezpieczeństwo produktów w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    OGÓLNEGO BEZPIECZEŃSTWA PRODUKTÓW)
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    do bezpieczeństwa i odszkodowania za uszkodzenie ciała lub rozstrój zdrowia
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    March 12, 2001
    Burger King and Alcone Recall Kid's Meal Toys

    Kids meal toy pictureMiami, FL (SafetyAlerts) - Burger King Corp. and Alcone Marketing Group, of Irvine, Calif., announced a recall today affecting about 400,000 "Rattling, Paddling Riverboat" toddler toys because of a potential choking hazard to young children. The toys were distributed in Burger King Kid's Meals. Metal pins with plastic caps that attach the paddle wheel to the riverboat toy can come out and pose a choking hazard.

    Burger King Corp. has received 10 reports that the pin on the toy came out. One child was found with the pin in her mouth. Her father removed it and no injuries have been reported.

    Alcone Marketing Group imported the toys for Burger King. The "Rattling, Paddling Riverboat" toys are red plastic boats about 2 to 3 inches in diameter. The captain figure squeaks when it is pushed down. When the boat is moved across the floor, beads in the boat's paddle wheel make a rattle sound. The following words are imprinted on the bottom of the boat, "Sassy, MFG FOR BURGER KING CORP, MADE IN CHINA." The packaging says "Toddler Toys For Kids Under Three Years Old."

    Burger King restaurants nationwide distributed the riverboat toys inside Kid's Meals in January and February 2001.

    Parents should immediately take the toy away from children and call (800) 661-9173 for instructions on returning the toy for a free, replacement toy. Information also is available at Burger King's web site at www.burgerking.com.


    Transgeniczna kukurydza w produktach firmy Kellogg Co.

    (WPŁYW ŻYWNOŚCI TRANSGENICZNEJ
    NA ŚRODOWISKO I ZDROWIE CZŁOWIEKA)
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    March 14, 2001
    Worthington Foods Recalls Corn Dogs

    Battle Creek, MI (SafetyAlerts) - Worthington Foods, a subsidiary of the Kellogg Co. is recalling all its meatless corn dogs after tests confirmed some of the product may contain the genetic material (DNA) necessary for the production in corn (trade name: StarLink) of the pesticide Cry9C protein derived from Bacillus thuringiensis subspecies tolworthi. The pesticide is not allowed for use in foods for human consumption.

    StarLink has not been approved for human consumption because of questions about its potential to cause human reactions. Government officials say there is little, if any, health risk for the corn.

    The recall includes all corn dogs sold under the names Morningstar Farms, Loma Linda, and Natural Touch. Consumers may call the company toll-free at 1-877-924-4247.


    Niedozwolona farba Acid Red 14  w produktach marki Nivea firmy Beiersdorf, Inc

    (jakość i skład kosmetyków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE KOSMETYKÓW)
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    March 14, 2001
    Nivea Mens Face Wash Recalled

    Norwalk, CT (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Beiersdorf, Inc. is recalling Nivea for Men-Double Action Face Wash (described further below) because the product contains the unapproved color additive acid red 14 (formerly certifiable as Ext. D&C Red No. 10).

    This is the first public notice of this Class II recall issued by FDA.

    PRODUCT
    a) Nivea for Men-Double Action Face Wash 5 Fl. OZ 150mL tube. Recall #F-292-1;
    b) Men's Grooming Kit containing Nivea for Men-Double Action Face Wash 0.5 Fl. OZ. 15 mL tube.

    Recall #F-293-1.

    CODE:
    All lots.

    MANUFACTURER:
    Beiersdorf, inc., Juvena, Germany.

    RECALLED BY:
    Beiersdorf, Inc., Norwalk, CT, by e-mail on 2/08/01 and by letter on
    2/14/01. Firm-initiated recall ongoing.

    DISTRIBUTION:
    Nationwide.

    QUANTITY:
    a) 5 fl. Oz.,  2,142 cases
    b) 0.5 fl. Oz. in kits, 33,000 cases.


    Bacillus licheniformis w paście do zębów firmy Colgate Palmolive

    (jakość i skład kosmetyków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE KOSMETYKÓW)
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    March 14, 2001
    Colgate Recalls 7,300 Cases of Toothpaste

    Jeffersonville, IN (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Colgate Palmolive  is recalling certain codes of toothpaste because of microbial contamination-(Bacillus licheniformis).

    Bacillus licheniformis is a Gram-positive, motile, spore-forming, facultatively anaerobic rod. Information regarding Bacillus licheniformis in relation to food safety is limited. Food poisoning by Bacillus licheniformis is characterised by diarrhoea, although vomiting occurs in half of reported cases.

    Bacillus licheniformis food poisoning has been associated with cooked meat, poultry and vegetable dishes (particularly stews and curries which have been served with rice).

     U.S. Government research has found that this organism normally is not harmful to people.

    This is the first public notice of this Class III recall issued by FDA.

    PRODUCTS
    a. Colgate Total Super Size 7.8 oz Toothpaste;
    b. Colgate Total Family size 6.0 oz Toothpaste;
    c. Colgate Great Regulator Flavor size 6.0 oz Toothpaste.

    Recall #D-140 - 141-1.

    CODES:
    a. SKU 74004, Exp. Date 03NOV02
    b. SKU 74003, Exp. Date 03NOV02
    c. SKU 72600, Exp. Date 03NOV02

    MANUFACTURER:
    Colgate Palmolive, Jeffersonville, IN.

    RECALLED BY:
    Colgate Palmolive, Piscataway, NJ, by FedEx letters and telephone on January 12, 2001. Firm-initiated recall ongoing.

    DISTRIBUTION:
    Nationwide.

    QUANTITY:
    a) Colgate Total Super size 7.8 oz -- 2813 cases
    b) Colgate Total Family size 6.0 oz -- 2700 cases
    c) Colgate Great Regular Flavor 6.0 oz -- 1862 cases.


    Zagrażające życiu kosiarki do trawy firmy Ariens, Scotts i Husqvarna

    (bezpieczeństwo produktów w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    OGÓLNEGO BEZPIECZEŃSTWA PRODUKTÓW)
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    do bezpieczeństwa i odszkodowania za uszkodzenie ciała lub rozstrój zdrowia
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    March 14, 2001
    Ariens, Scotts, and Husqvarna Lawn Mowers Recalled

    Ariens, Scotts, and Husqvarna Lawn Mowers RecalledBrillion, WI (SafetyAlerts) - In cooperation with the U.S. Consumer Product Safety Commission (CPSC), Ariens Co. is recalling about 40,000 walk-behind lawn mowers sold under the Ariens, Scotts, and Husqvarna brand names. The piece attaching the blade to the mower can crack and break off. The broken piece or the blade can be propelled from underneath the mower, possibly injuring the operator or a bystander.

    Ariens Co. has received four reports of the broken piece or detached blade being propelled from underneath the mower. One consumer was struck in the leg and received a bruise.

    The recalled Ariens, Scotts, and Husqvarna rotary lawn mowers are walk- behind, 21-inch gas-powered mowers. The Ariens mower has an orange mower deck with black handlebars. The Husqvarna and Scotts mowers have an orange mower deck with gray handlebars. A label on the top of the deck area behind the engine of the mowers has the following model and serial numbers:
     

       
       
      Model Number Serial Number
      Scotts model #907254 serial numbers 101 to 019124
      Ariens model #911513 serial numbers 101 to 001242
      Ariens model #911514 serial numbers 101 to 006616
      Ariens model #911515 serial numbers 101 to 001445
      Ariens model #911516 serial numbers 101 to 005105
      Husqvarna model #601100020 serial numbers 101 to 003115
      Husqvarna model #601100021 serial numbers 101 to 000720 and
      serial numbers 2301 to 002576
      Husqvarna model#601100022 serial numbers 101 to 002797


    Ariens and Husqvarna dealers, and department and home center stores, including Home Depot (which only sold the Scotts brand), sold these mowers nationwide from December 1999 through October 2000 for between $360 and $800.

    Consumers should stop using these recalled mowers immediately and return them to an authorized dealer for free repair. To locate the nearest dealer or for more information, call Ariens toll-free at (877) 740-7060 between 7:30 a.m. and 4:40 p.m. CDT Monday through Friday. Consumers also can go to the Ariens web site at www.ariens.com/lawn_safety_recall/ or the Husqvarna web site at http://www.husqvarna.com/news/shl_news.htm.
     


    Bacillus licheniformis w preparacie aptecznym Fast-Acting Antacid Anti-gas
    firmy Aaron Industries, Inc.

    (jakość i skład leków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    ŚRODKÓW FARMACEUTYCZNYCH
    I MATERIAŁÓW MEDYCZNYCH)

    \\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\\
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    do bezpieczeństwa i odszkodowania za uszkodzenie ciała lub rozstrój zdrowia
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    March 14, 2001
    California Firm Recalls Fast-Acting Antacid

    Lynwood, CA (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Aaron Industries, Inc. is recalling its Pharmacy’s Prescription, Fast-Acting Antacid Anti-gas because of microbial contamination-(Bacillus licheniformis).

    Bacillus licheniformis is a Gram-positive, motile, spore-forming, facultatively anaerobic rod. Information regarding Bacillus licheniformis in relation to food safety is limited. Food poisoning by Bacillus licheniformis is characterised by diarrhoea, although vomiting occurs in half of reported cases.

    Bacillus licheniformis food poisoning has been associated with cooked meat, poultry and vegetable dishes (particularly stews and curries which have been served with rice)

    This is the first public notice of this Class II recall issued by FDA.Bacillus licheniformis

      PRODUCT
    Pharmacy’s Prescription, Fast-Acting Antacid Anti-gas, Original Flavor, 12 fl oz.

    Recall #D-139-1.
    z
    CODE:
    Lot Number C-1188, Antacid Anti-Gas, Pharmacy’s Prescription Brand, NDC 49580-0106-2.

    MANUFACTURER:
    Aaron Industries, Inc., Lynwood, CA.

    RECALLED BY:
    Manufacturer, by telephone and letter. Firm-initiated recall ongoing.

    DISTRIBUTION:
    KY,CA, TN, NY.

    QUANTITY:
    10,498 units.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


    Zatajone białko i żółtko jaja oraz zatajone farby
    w zestawach wegetariańskich firmy Silver Creek Fresh, Inc.

    (NIEPOŻĄDANE REAKCJE NA PRODUKTY SPOŻYWCZE,
    (dawki E 102, E 110  i E 129 w polskich produktach:
    BARWNIKI ŻYWNOŚCI I NAPOJÓW)
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    March 14, 2001
    FDA First Notice: Veggie and Nacho Trays Recalled

    Garden City, ID (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Silver Creek Fresh, Inc. has recalled certain Veggie Trays and Nacho Trays because the veggie trays contain undeclared egg yolks, and the nacho trays contain undeclared eggs, egg yolks, FD&C Yellow No. 5, and No. 6, FD&C Red No. 40 and FD&C Blue No. 1.

    This is the first public notice of this Class I recall issued by FDA.

    PRODUCT
    a) Silver Creek Fresh Prep Mini Veggie Trays. Recall #F-279-1;
    b) Super Nacho Trays. Recall #F-280-1.

    CODE:
    a & b) Best used by dates September 14 and prior.

    MANUFACTURER:
    Silver Creek Fresh Prep, Rupert, ID., and Quality Produce, Garden City, ID.

    RECALLED BY:
    Silver Creek Fresh, Inc., Garden City, ID., by faxed letter and press release on 9/8/00. Firm-initiated recall *complete.

    *Completed recall: FDA states 'completed recall' indicates the company has removed all affected product from store shelves,  it does not necessarily mean this particular product lot, or codes, have been fully accounted for.

    DISTRIBUTION:
    Utah, Idaho, Nevada, Wyoming and Montana.

    QUANTITY:
    a) 342 cases; b) 137 cases.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


    Zatajone orzechy ziemne w produktach nowojorskiej piekarni

    (NIEPOŻĄDANE REAKCJE NA PRODUKTY SPOŻYWCZE)
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    March 15, 2001
    Allergy Alert: New York Bakery Recalls Canaan Bakery Cookies

    Albany, NY (SafetyAlerts) - New York State Agriculture Commissioner Nathan L. Rudgers has announced that Canaan Bakery Number Three Corporation, is recalling Canaan Bakery Cookies because the product contains undeclared peanuts.

    No illnesses have been reported to date in connection with this product.

    People who have allergies to peanuts run the risk of a serious or life threatening allergic reaction if they consume this product.

    The recalled product "Canaan Bakery Cookies" is packaged in a plastic tube weighing approximately 6 oz. The package is not coded, nor is there an ingredient listing.

    The product was sampled by the New York State Department of Agriculture and Markets food inspectors during a routine inspection of the establishment. Canaan Bakery Number Three Corporation indicates the product was distributed in Queens only.

    Consumers who have purchased this product are urged to return it to the place of purchase.


    Amoniak w produktach firmy Camino Real Foods Inc.

    (POLSKIE PRZEPISY SANITARNE
    DOTYCZĄCE ARTYKUŁÓW SPOŻYWCZYCH)
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    Twoje prawo
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    March 31, 2001
    Tina's Red Hot Frozen Beef Burritos Recalled

    Vernon, CA (SafetyAlerts) - Camino Real Foods Inc. is voluntarily recalling certain lots of its five-ounce Tina's Red Hot Beef burritos, because the product may be contaminated with a commonly used Ammonia-based refrigerant.

    The company stated that levels of contamination were relatively small, measured in parts per million, and had the primary effect of a noticeably bad taste in some of the contaminated burritos.  Additionally, the company press release noted there are no known long-term health effects associated with this level of exposure to the Ammonia-based refrigerant. In some cases, there may be temporary irritation of the mouth, throat and gastrointestinal tract.

    The product subject to recall was the five-ounce Tina's Red Hot Beef burritos that were distributed to Utah, Arizona and Southern California.

    Consumers who purchased these burritos between March 12 and March 30, with a date code of V10603 or U10603, may return the product to the retailer from which it was purchased for a full refund.


    Zatajona serwatka i żółtko jaja w produktach drobiowych firmy Simmons Foods

    (NIEPOŻĄDANE REAKCJE NA PRODUKTY SPOŻYWCZE)
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    March 31, 2001
    Simmons Foods Recalls 5.5 Million Pounds of Chicken Breast Strips for Undeclared Allergen

    Van Buren, AR (SafetyAlerts) - Simmons Foods is voluntarily recalling approximately 5.5 million pounds of chicken breast strips because they contain undeclared allergens (whey and egg yolks), the U.S. Department of Agriculture’s Food Safety and Inspection Service announced today.

    Whey and egg yolks are known allergens. Persons who have an allergy or severe sensitivity to the whey or egg yolks run the risk of possible allergic reactions if they consume this product.

    The products being recalled are "GRILLED CHICKEN BREAST STRIPS WITH RIB MEAT" packaged in case numbers 50054, 60054, 50055, and 50118. All cases are labeled with the plant number P-20287.

    The products were distributed to restaurants and institutions nationwide.

    "FSIS ensures that meat and poultry products are safe, wholesome, and accurately labeled," said Thomas J. Billy, administrator of FSIS. "Consumers who have concerns should return the products to the point of purchase."

    The problem was discovered by the establishment, which then notified FSIS. FSIS is not aware of any illnesses associated with consumption of the product. Anyone concerned about an illness should contact a physician immediately.

    Consumers with questions about the recall may contact David Harris, director of quality assurance, Simmons Foods, at (501) 524-8151, ext. 426. Media with questions about the recall may contact Todd Simmons, president, Simmons Foods, at (501) 524-8151, ext. 244.

    Consumers with other food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time), Monday through Friday, and recorded food safety messages are available 24 hours a day.


    Zatajona serwatka i żółtko jaja w produktach drobiowych firmy Keystone Foods
    (NIEPOŻĄDANE REAKCJE NA PRODUKTY SPOŻYWCZE)
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    March 31, 2001
    Keystone Foods Recalls 3.7 Million Pounds of Chicken Breast Strips

    Gadsden, AL (SafetyAlerts) - Keystone Foods is voluntarily recalling approximately 3.7 million pounds of chicken
    breast strips because they contain undeclared allergens (whey and egg yolks), the U.S. Department of Agriculture’s Food Safety and Inspection Service announced today.

    Whey and egg yolks are known allergens. Persons who have an allergy or severe sensitivity to the whey or egg yolks run the risk of possible allergic reactions if they consume this product.

    The products being recalled are "FULLY COOKED GRILLED CHICKEN BREAST STRIPS WITH RIB MEAT" packaged in case numbers 50054, 5005430K, and 5005440G. All cases are labeled with the plant number P-17341.

    The products were distributed to restaurants and institutions in Kentucky, Virginia, Florida, New Jersey, North Carolina, New York, California, and Texas.

    "FSIS ensures that meat and poultry products are safe, wholesome, and accurately labeled," said Thomas J. Billy, administrator of FSIS. "Consumers who have concerns should return the products to the point of purchase."

    The problem was discovered by the establishment, which then notified FSIS. FSIS is not aware of any illnesses associated with consumption of the product. Anyone concerned about an illness should contact a physician immediately.

    Consumers and media with questions about the recall may contact Allison Appleby, food safety quality assurance manager with Keystone Foods, at (256) 492-4050.

    Consumers with other food safety questions can phone the toll-free USDA Meat and Poultry Hotline at 1-800-535-4555. The hotline can be reached from 10 a.m. to 4 p.m. (Eastern Time), Monday through Friday, and recorded food safety messages are available 24 hours a day.


    Brak ostrzeżenia zdrowotnego na opakowaniu niskokalorycznego napoju zawierającego aspartam

    (POLSKIE PRZEPISY SANITARNE
    DOTYCZĄCE ARTYKUŁÓW SPOŻYWCZYCH)
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    April 4, 2001
    FDA First Notice: Dairymen's Lemon Flavor Diet Iced Tea Recalled

    Ferndale, MI (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Oberlin Farms Dairy, Inc. has recalled Dairymen's Lemon Flavor Diet Iced Tea because the product contained aspartame but did not bear the warning statement "PHENYLKETONURICS: CONTAINS PHENYLALANINE" as required by 21CFR 172.804.

    This is the first public notice of this Class III recall issued by FDA.

    PRODUCT
    Dairymen's Lemon Flavor Diet Iced Tea in 1 pt. and 1/2 gallon containers.

    Recall #F-311-1.

    CODE:
    All Sell-By Dates from 2/9/01 through 3/28/01.

    MANUFACTURER:
    Oberlin Farms Dairy, Inc., Cleveland, OH.

    RECALLED BY:
    Manufacturer, by letter dated 2/9/01. FDA initiated recall
    *complete.

    DISTRIBUTION:
    Ohio, Michigan & Pennsylvania.

    QUANTITY:
    7000 Gallons.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


    Kwas arystolochowy w preparatach ziołowych firmy Green Kingdom Herbs

    (jakość i skład leków w Polsce:
    POLSKIE PRZEPISY DOTYCZĄCE
    ŚRODKÓW FARMACEUTYCZNYCH
    I MATERIAŁÓW MEDYCZNYCH)
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    April 4, 2001
    FDA First Notice: Green Kingdom Herbs Recalls 13 Varieties of Herb Products

    Bay City, MI (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Green Kingdom Herbs has recalled 13 varieties of herb products because the products contained aristolochic acid, a potent carcinogen and nephrotoxin.

    This is the first public notice of this Class I recall issued by FDA.

    PRODUCT
    All Green Kingdom Herbs products of the following varieties (listed with Latin name of botanical):

    a)Akebia Extract, (akebia trifoliata). Recall #F-321-1;

    b)Stephania Extract, (stephania tetrandra). Recall #F-322-1;

    c)Clematis (Chinese) Extract, (clematis chinensis). Recall #F-323-1;

    d)Virginia Snake Root Extract, (aristolochia serpentaria).
    Recall #F-324-1;

    e)Witch Hazel Formula, (containing Virginia Snake Root
    Extract, aristolochia serpentaria). Recall #F-325-1;

    f)PFC - custom made formula, (containing Virginia Snake
    Root Extract, aristolochia serpentaria). Recall #F-326-1;

    g)HPX - custom made formula, (containing Virginia Snake Root Extract, aristolochia serpentaria). Recall #F-327-1;

    h)Ligusticum & Green Tea Formula I, (containing asarum). Recall #F-328-1;

    i)Ligusticum & Green Tea Formula II, (containing asarum). Recall #F-329-1;

    j)Ligusticum & Green Tea Formula III, (containing asarum). Recall #F-330-1;

    k)Ligusticum & Green Tea Formula IV, (containing asarum). Recall #F-331-1;

    l)Ligusticum & Green Tea Formula V, (containing asarum). Recall #F-332-1;

    m)Minor Blue Dragon Combination, (containing asarum).
    Recall #F-333-1.

    CODES:
    All Lots.

    MANUFACTURER:
    Green Kingdom Herbs, Bay City, Michigan.

    RECALLED BY:
    Manufacturer, via telephone and certified mail on December 1, 2000, and by press release November 21, 2000. Firm-initiated recall *complete.

    *Completed recall: FDA states 'completed recall' indicates the company has removed all affected product from store shelves,  it does not necessarily mean this particular product lot, or codes, have been fully accounted for.

    DISTRIBUTION:
    Michigan, Texas, Georgia, Indiana, Illinois, New York, California.

    QUANTITY:
    a) 3 (three) 4oz. Bottles;
    b) 3 (three) 8oz. Bottles;
    c) 3 (three) 4oz. Bottles;
    d) 12 (twelve) 1oz. bottles, 8 (eight) 4oz.bottles, 2 (two) eight oz. bottles, 1 (one) ˝ gallon container;
    e) 2 (two) 1oz. Bottles;
    f) 37 gallons, 12 oz.;
    g) 13 gallons, 50 oz.;
    h) 3 (three) 1oz. bottles, 3 (three) 4oz. Bottles;
    i) 3 (three) 1oz. Bottles;
    j) 3 (three) 1oz. Bottles;
    k) 3 (three) 1oz. bottles, 1 (one) 4oz. Bottle;
    l) 4 (four) 1oz. bottles, 1 (one) 4oz. Bottle;
    m) 1(one) 4oz. Bottle.

    Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.


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    ALARM KONSUMENCKI
    - FIRMY, MARKOWE PRODUKTY, ZAGROŻENIA ZDROWIA - CZ. IV
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