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07-02-2013, 10:18 PM #1
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- Aug 2012
- Merced, CA 95348-1422
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Florida Firm Recalls Blue Cheese Chicken Dip Products Due To Misbranding And Undecl
Florida Firm Recalls Blue Cheese Chicken Dip Products Due To Misbranding And Undeclared Allergen
Class II Recall 042-2013
Health Risk: Low Jun 26, 2013
Congressional and Public Affairs
Peggy Riek (202) 720-9113
WASHINGTON, June 26, 2013 – ECRS, LLC, a Hollywood, Fla., establishment, is recalling 12,560 pounds of chicken dip products because of misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service announced today. The products contain anchovies, a known allergen which is not declared on the label.
The products subject to recall include:
8-oz. containers with 16 pieces per case of “BUBBA’S Buffalo Blue Cheese Chicken Dip” bearing the establishment number “P-21299” inside the USDA mark of inspection. The products were produced and packaged on April 10, 2013.
16-oz. containers with 8 pieces per case of “BUBBA’S Buffalo Blue Cheese Chicken Dip” bearing the establishment number “P-21299” inside the USDA mark of inspection with expiration dates from June 25, 2013, through Sep. 24, 2013. The products were produced and packaged from March 21, 2013, through June 21, 2013.
The products were distributed to retail grocery stores and through internet/catalog sales in Florida, Georgia, Illinois, Missouri and Ohio.
The problem was discovered by an FSIS inspector who conducted a label review which was prompted by the April 30, 2013, release of FSIS Notice 29-13. FSIS took the step of issuing the FSIS notice in an effort to protect vulnerable consumers after observing an increase in the number of products recalled from 2008 through 2012 due to the presence of undeclared allergens or other ingredients. FSIS personnel are responsible for verifying that establishments are actively labeling the eight most common food allergens. The problem occurred when the plant began formulating the product using a dressing containing anchovies and did not make the necessary change to the product label.
FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.
FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Media and consumers with questions about the recall should contact Charlie Gonzalez, Manager, at (954) 965-2480.