FDA recall record

Seabear Company Banquet Cut European Style Cold Smoked Salmon, Item Number recall — FDA F-1009-2021

Potential for growth of C. botulinum

Class IIclassification
F-1009-2021official record ID
Sep 29, 2021report date

Recall record at a glance

Official recordF-1009-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSeabear Company
Report dateSep 29, 2021
Recall initiation dateSep 8, 2021
Quantitytotal 126 cases (756 pouches)
LocationAnacortes, WA, United States

Official product description

Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in pouch, net wt. per pouch is random, frozen, UPC of pouch: 2 92845 00250 3. The storage/thawing instructions on the pouch is read in parts: "***KEEP FROZEN UNTIL USED. THAW UNDER REFRIGERATION AT OR BELOW 38F. USE BY 30 DAYS AFTER THAW***". The master case has the UPC 7 52047 92845 7 and net wt. 16 lbs. The master case label is read in parts: LOX EURO SLICED BANQUET 6/CS ***2-92845 *** Ingredients: Smoked Salmon (Atlantic Salmon, salt, cane sugar, spices, natural wood smoke)***Contains: Astaxanthin or Canthaxanthin. Contains: Salmon***Important, keep frozen until used, thaw under refrigeration at 38F or below*** Use By 30 Days After Thaw ***".

Why the product was recalled

Potential for growth of C. botulinum

Distribution information

distributed in AZ, CA, and GA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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