FDA RECALLS
Maru Bakery & Wholesale Recalls Elsa Kolo Roasted Barley
Contact:
-- Maru Bakery & Wholesale, Dallas, TX is recalling Elsa Kolo Roasted Barley because it contains undeclared peanuts.
The recalled Roasted Barley sold in 3 oz, ½ lb, 5 lb and 10 lb clear plastic bags, with or without labels, were sold in Dallas, TX, Houston, TX, Atlanta, GA and Columbus, OH. The bags with labels identify the product as Elsa Kolo Roasted Barley. The product was also distributed in bulk 88 lb white bags that are labeled "Maru Import & Export Dallas, Texas U.S.A Item Elsa Kolo".
People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.
The recall was initiated after a routine FDA inspection revealed the presence of peanuts in packages of roasted barley.
No illnesses have been reported to date in connection with this problem.
Consumers who have purchased Elsa Kolo Roasted Barley should return it to the place of purchase. Consumers with questions may contact the company at 214-221-3123
This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html
Consumer Alert: Undeclared Sulfites In Dried Mushrooms
New York State Agriculture Commissioner Patrick H. Brennan today alerted consumers that Korica International Inc., 98 Bay 35 Street, Brooklyn, New York 11214, is recalling certain "Dried Mushrooms" due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
The recalled "Dried Mushrooms" are packaged in a 5-ounce, uncoded, plastic bag. They were sold nationwide. They are a product of China.
Routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel revealed the product contained high levels of sulfites which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites.
No illnesses have been reported to date to this Department in connection with this problem.
Consumers who have purchased "Dried Mushrooms" should return them to the place of purchase
Target® Issues Allergy Alert on Undeclared Egg in SuperTarget™ & Archer Farms™ Mini Angel Food
Contact:
Target Media Relations
1-612-696-3400
Target®, headquartered in Minneapolis, MN, is recalling SuperTarget™ brand Mini Angel Food cakes that were purchased before August 5, 2006 as they contain an undeclared Dried Egg White ingredient. This item may have an ARCHER FARMS™ sticker on the package. People with an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product. The recalled item is:
SuperTarget or ARCHER FARMS Mini Angel Food 6-pack, 9.52 oz
Sell By dates prior to 08/15/06 (printed on the white label)
Affected UPC Codes include 59608-00465, 32479-20399, 32479-30350, 32479-60299, 32479-70349, 32479-80798
The recalled item was sold at SuperTarget retail stores nationwide within the in-store Bakery area.
One illness has been reported to date in connection with this problem. Anyone concerned about an illness related to this product should contact a physician immediately.
Upon awareness of the issue, the ingredient statement was corrected to include the missing Dried Egg White ingredient. Product with Sell By dates of 08/15/06 and after have the corrected ingredient statement which includes Dried Egg White and also lists Egg within the allergen Contain statement.
Consumers who have purchased this item are urged to return it to the place of purchase for a full refund. Consumers with questions may contact Target Guest Relations at 1-800-316-6151.
The Mentholatum Company Issues a Nationwide Voluntary Recall of WellPatch® Cough & Cold Soothing Vapor Pads in the U.S.
The Mentholatum Company announced today it is conducting a nationwide voluntary recall of WellPatch® Cough & Cold Soothing Vapor Pads due to potential serious adverse health effects that could result if the product is ingested by a child removing the patch and chewing on it.
Consumers who have WellPatch® Cough & Cold Soothing Vapor Pads should stop using them immediately. The Mentholatum Company is taking this precautionary action to ensure the safety of the consumers who use this product. To date, there have been no serious adverse events reported.
The Mentholatum Company is initiating the recall due to the possibility of adverse events associated with use of the product. WellPatch® Cough & Cold Soothing Vapor Pads contain camphor, eucalyptus oil, and menthol. Possible adverse events associated with chewing or ingesting products containing camphor or eucalyptus oils can vary from minor symptoms, such as burning sensation in the mouth, headache, nausea and vomiting, to more severe reactions, such as seizures.
The recall is being conducted with the knowledge of the FDA. WellPatch® Cough & Cold Soothing Vapor Pads are labeled for use by children two (2) years of age and older. The directions on the label indicate the patch is to be applied to the throat or chest to allow the vapors to reach the nose and mouth. Once applied, the patch would be within close reach for a child to remove and place in his/her mouth. The Vapor Pad is a topical cough product applied externally and not intended for oral consumption.
The product is sold nationwide over-the-counter at pharmacies and retail stores. This recall affects only the Cough & Cold Soothing Vapor Pads. Consumers should immediately discontinue use of this product and return it to their point of purchase for a full refund or discard it. Consumers requiring more information about this recall can contact The Mentholatum Company Customer Service Department at 1-877-636-2677 or visit www.wellpatch.com.
Any adverse reactions experienced with the use of this product should also be reported to the FDA's MedWatch Adverse Event Reporting program online [at http://www.fda.gov/medwatch/report.htm], by phone [1-800-FDA-1088], or by returning the postage-paid FDA form 3500 [which may be downloaded from http://www.fda.gov/medwatch/getforms.htm] by mail [to MedWatch, 5600 Fishers Lane, Rockville, MD 20852-9787] or fax [1-800-FDA-0178].
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