1) Chicken of the Sea Whole Oysters Pieces 24 units per case, UPC 4800000069; 2) Pacific Pearl Whole Oysters Pieces 12 units per case, UP...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1433-2012.
Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under the Chicken of the Sea, Pacific Pearl, and Ace of Diamonds brands because the products have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1433-2012.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Tri-union Seafoods, L.l.c Dba Chicken Of The Sea. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1433-2012.
Tri-Union Seafoods, L.L.C dba Chicken of the Sea.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Tri-union Seafoods, L.l.c Dba Chicken Of The Sea. Recall FAQ
Tri-union Seafoods, L.l.c Dba Chicken Of The Sea. is the subject of a meat & poultry safety report: 1) Chicken of the Sea Whole Oysters Pieces 24 units per case, UPC 4800000069; 2) Pacific Pearl Whole Oysters Pieces 12 units per case, UP.... The notice was published on May 26, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 1 units are potentially affected.