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Showing posts with label FDA. Show all posts
Showing posts with label FDA. Show all posts

Thursday, October 27, 2011

Turkish Pine Nuts Recalled due to Salmonella




Wegmans Food Markets, Inc. Announces Recall of Bulk Turkish Pine
Nuts Due to Possible Salmonella Contamination


Contact:
Consumer:
1(800) WEGMANS (934-6267)

Media:
585.429.3627
jo.natale@wegmans.com 
 
FOR IMMEDIATE RELEASE - October 26, 2011 - Rochester, NY - Wegmans Food Markets, Inc. is recalling approximately 5,000 lbs. of Turkish Pine Nuts sold in the Bulk Foods department of most Wegmans stores in New York, Pennsylvania, New Jersey, Virginia, and Maryland between July 1 and October 18, 2011 due to possible Salmonella contamination.

The bulk Turkish Pine Nuts have been linked to an outbreak of illness from Salmonella Enteritidis, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. Illness onset is typically 12 to 72 hours after consumption.

This recall only applies to Turkish Pine Nuts sold in bulk. Other pine nuts sold at Wegmans are not affected by this recall.

The recalled Turkish pine nuts were imported from Turkey by Sunrise Commodities of Englewood Cliffs, N.J.

The recalled product was not sold at the company’s Northborough, Massachusetts store, which opened on Sunday, October 16.

The recall was initiated as a result of a multi-state outbreak investigation by the Centers for Disease Control and Prevention (CDC) (www.cdc.gov/salmonella). Wegmans is working closely with the CDC, the Food and Drug Administration (FDA), and state and local public health and agriculture officials on this matter.

Wegmans has placed automated phone calls to customers who purchased the Turkish Pine Nuts using their Shoppers Club card alerting them about the recall.

Consumers who have purchased this product should discard any that remains in their homes and visit the service desk at Wegmans for a full refund. Consumers with questions may contact Wegmans consumer affairs department toll free at 1(800) WEGMANS (934-6267) Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time.

Wegmans Food Markets, Inc. is a 79-store supermarket chain with stores in New York, Pennsylvania, New Jersey, Virginia, Maryland, and Massachusetts.

Tuesday, October 25, 2011

Frozen Egg Products Recalled due to Salmonella




American Egg Products 

Recalls Frozen Egg Product Because Of Possible Health Risk


Contact:
Consumer:
Jim Hull
(912) 449-5700
FOR IMMEDIATE RELEASE - October 24, 2011 -American Egg Products of Blackshear, Georgia, is recalling five pound cartons of frozen egg product, Lot #272-1, because they may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonellaoften experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection withSalmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The recalled egg product was distributed to Georgia and Florida and sold to three distributors and/or further food manufacturers.

The product, American Egg Products Frozen Egg Product, comes in five pound paper cartons. Lot # 272-1 is printed across the side of the master case and is also embossed on the gable of each individual carton inside the case with the plant number as 272 1 P 1105.

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

The recall was initiated as a result of a routine sampling by a private laboratory which revealed that the finished product containedSalmonella.  The company has ceased distribution of the above referenced product.  Investigation by the FDA and the company is ongoing to identify the source of the problem.

Consumers who have purchased this product, American Egg Products Frozen Egg Product, Lot # 272-1, are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 912-449-5700 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time.

Saturday, September 17, 2011

FDA Oral Contraceptives Recalled!

Qualitest Pharmaceuticals Oral Contraceptives: Recall - Packaging Error 
Includes the following medications:
  • Cyclafem 7/7/7
  • Cyclafem 1/35
  • Emoquette
  • Gildess FE 1.5/30
  • Gildess FE 1/20
  • Orsythia
  • Previfem
  • Tri-Previfem
AUDIENCE: Consumer, Pharmacy, OB/GYN

ISSUE: Qualitest Pharmaceuticals issued a nationwide, retail-level recall of multiple lots of oral contraceptives because a packaging error may result in the daily regimen for these products being incorrect and could leave women without adequate contraception, and at risk for unintended pregnancy. Select blisters were rotated 180 degrees within the card, reversing the weekly tablet orientation and making the lot number and expiry date no longer visible.

BACKGROUND: These packaging defects do not pose any immediate health risks. Pharmacies are being instructed to contact consumers who have received affected product.

RECOMMENDATION: Consumers exposed to affected packaging should begin using a non-hormonal form of contraception immediately and consult their health care provider or pharmacist. Consumers who have affected products should contact Qualitest for information or to arrange return of any affected product.

Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:

  • Complete and submit the report Online: www.fda.gov/MedWatch/report.htm
  • Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178