Update on Tainted Veggie Booty Snack Food
FDA Testing Confirms Presence of Salmonella Contamination
The Food and Drug Administration (FDA) today confirmed that a strain of Salmonella Wandsworth bacteria found in Veggie Booty snack food is responsible for the disease outbreak that occurred between March and June 2007.
Epidemiological testing conducted by the Minnesota Agricultural Lab previously implicated Veggie Booty snack food as the source of the outbreak. The results of FDAís own testing added confirmation.
Veggie Booty is marketed by Robertís American Gourmet, of Sea Cliff, N.Y.
FDA continues to advise consumers not to eat any Veggie Booty and to throw away product they have. FDA also advises consumers not to eat Super Veggie Tings Crunchy Corn Sticks, and to throw out any supplies they have, because this product also may be contaminated.
No illnesses have been associated with any other Robertís American Gourmet products.
Salmonella typically causes diarrhea (may be bloody), often accompanied by abdominal cramps and fever. Symptoms typically begin within one to four days after exposure to the bacteria. In infants and persons with poor underlying health and those with weakened immune systems, Salmonella can invade the bloodstream and cause life-threatening infections.
Individuals who have recently eaten Veggie Booty or Super Veggie Tings Crunchy Corn Sticks and who have experienced any of the symptoms described below should contact a doctor or other health care provider immediately. Both products may appeal to children, so parents should be especially vigilant and seek medical care if they observe signs of illness.
The Centers for Disease Control and Prevention (CDC) has identified 60 children from 19 states who have become ill. Six children were hospitalized. There are no reported deaths. States reporting illnesses include: California (seven cases), Colorado (five), Connecticut (two), Georgia (one), Illinois (one), Indiana (one), Massachusetts (four), Minnesota (two), New Hampshire (two), New Jersey (two), New York (15), Oregon (one), Pennsylvania (four), Tennessee (one), Texas (two), Virginia (one), Vermont (three), Washington (four), and Wisconsin (two).
FDA, the States, and CDC are continuing the investigation. Preliminary testing suggests that the seasoning mix used in Veggie Booty may be the source of the contamination. FDA will continue to trace back the ingredients and processing methods used for the seasoning mix, seeing to determine whether the seasoning actually is the source of the problem.
Veggie Booty is sold in a flexible plastic foil bag in four ounce, one ounce and one-half ounce packages. Some gift baskets available for purchase on the internet include Veggie Booty or Super Veggie Tings Crunchy Corn Sticks.
Robertís American Gourmet ceased distributing Veggie Booty and began recalling the product on June 28. The company has also voluntarily recalled all lots and sizes of Super Veggie Tings Crunchy Corn Sticks snack food because the same potentially contaminated seasoning may have been used in making that product, too. In addition, the manufacturer of Veggie Booty and other products for Robertís has ceased production until this investigation is complete. Robertís American Gourmet and its contract manufacturer are fully cooperating with FDAís investigation into the cause of the contamination.
FDA will provide additional updates as the investigation progresses and more information becomes available.
Wellbaskets.com Is Alerting Customers of the Veggie Booty Voluntary Recall Issued on June 28, 2007 by Robertís American Gourmet (July 2, 2007)
Robertís American Gourmet Food, Inc. Conducts a Nationwide Recall of Super Veggie Tings Crunchy Corn Sticks Because of Possible Health Risk (July 2, 2007)
Photo: Robertís American Gourmet Super Veggie Tings Crunchy Corn Sticks
FDAís Pilot Program to Better Educate Consumers about Recalled Food Products
Robertís American Gourmet Food, Inc. Conducts Nationwide Recall of Veggie Booty Because of Possible Health Risk (June 28, 2007)
Veggie Booty Snack Food Identified in Product Recall (June 28, 2007)
FDA Press Release (June 28, 2007)
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