FDA News

Recall of Patak's Dopiaza Cooking Sauce (September 4)

ACH Food Companies, Inc. is recalling its Patak's Dopiaza Cooking Sauce sold in the United States because it may contain an undeclared milk allergen. People who have an allergy or severe sensitivity to milk may run the risk of serious or life-threatening allergic reaction if they consume these products. The product is distributed nationally through retail stores. ACH Food Companies is notifying its distributors and stores that carry this product that it contains an undeclared milk allergen and to immediately remove it from distribution.

Sprouters Northwest, Inc. Recalls Alfalfa Sprout Products Because of Possible Health Concern (September 5)

Sprouters Northwest, Inc. of Kent, Washington is recalling its alfalfa sprout products (alfalfa sprouts, onion sprouts, and salad sprouts) because they may be linked to a recent outbreak of Salmonellosis in Oregon and Washington State. To date, 13 cases of Salmonella Typhimirium infection have been associated with the consumption of raw alfalfa sprouts.

T. Marzetti Company Recalls a Limited Number of Girard's Honey Dijon Peppercorn (September 4)

T. Marzetti Company is recalling a limited number of 12 fl. oz. bottles of Girard's Honey Dijon Peppercorn (item 58105) because they may have the incorrect back label of Girard's French Dressing (item 58015). The Girard's Honey Dijon Peppercorn contains eggs, which is not declared as an ingredient on the Girard's French label. People who have allergies to egg run the risk of serious allergic reaction if they consume this product.

Potential Signals of Serious Risks/New Safety Information Identified by the Adverse Event Reporting System (AERS)

Potential Signals of Serious Risks/New Safety Information Identified by the Adverse Event Reporting System (AERS)

Potential Signals of Serious Risks/New Safety Information Identified by the Adverse Event Reporting System (AERS): January - March 2008

Potential Signals of Serious Risks/New Safety Information Identified by the Adverse Event Reporting System (AERS): January - March 2008

Adverse Event Reporting System (AERS) (updated)

Adverse Event Reporting System (AERS) (updated)

FDA to Post Quarterly Report of Potential Safety Issues

The U.S. Food and Drug Administration announced today that it has posted on its Web site its first quarterly report that lists certain drugs that are being evaluated for potential safety issues. The drugs have been identified based on a review of reports in FDA's Adverse Event Reporting System (AERS).

The Hershey Company Announces Nationwide Voluntary Recall of Hershey's Chocolate Shell Topping Due to Undeclared Almonds (September 4)

The only 7.25-ounce bottles of Hershey's Chocolate Shell Topping affected have the code 69N printed on the back of the bottle below the UPC symbol. The UPC/Bar Code is 346000. The item in question was available for purchase nationwide after July 8, 2008.

Starway Inc. Issues Alert on Undeclared Sulfites in Ego Brand Preserved Peaches (September 3)

EGO brand Preserved Peaches is sold in a 14 ounce, un-coded, clear plastic package and was distributed nationwide. It is a product of Malaysia.

Tumor necrosis factor-α blockers (TNF blockers), Cimzia (certolizumab pegol), Enbrel (etanercept), Humira (adalimumab), and Remicade (infliximab)

Opportunistic infections are not consistently recognized in patients taking tumor necrosis factor-α blockers.

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