Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water, 48 cans per case, UPC code is 0 4800000245 7
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1065-2016.
Tri-Union Seafoods LLC is voluntarily recalling a limited amount of Chicken of the Sea brand 5 oz. canned chunk light tuna in oil and 5 oz. canned chunk light tuna in water. This recall has been initiated because the product may have been undercooked due to an equipment malfunction, which was uncovered during a routine inspection.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1065-2016.
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-1065-2016.
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.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
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: Chicken of the Sea 5 Oz. Canned Chunk Light Tuna in Water, 48 cans per case, UPC code is 0 4800000245 7. The notice was published on March 17, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 1,501 units are potentially affected.