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Food FDA Class II Terminated Pathogen contamination

SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.

Seabear Company Published Apr 9, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 75/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Seabear Company or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.

Hazards

Clostridium botulinum · primary

Affected products (1)

SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.

Salmon Chowder = 11,152 pouches

Code info: 64242902SALCH Enjoy by: 10/2028 64242912SALCH Enjoy by: 10/2028 64242972SALCH Enjoy by: 10/2028 64242982SALCH Enjoy by: 10/2028 64243042SALCH Enjoy by: 10/2028 64243052SALCH Enjoy by: 10/2028 64243121SALCH Enjoy by: 11/2028 64243131SALCH Enjoy by: 11/2028 64243191SALCH Enjoy by: 11/2028 64243201SALCH Enjoy by: 11/2028 64243651SALCH Enjoy by: 12/2028 64250031SALCH Enjoy by: 1/2029 64250291SALCH Enjoy by: 1/2029 64250301SALCH Enjoy by: 1/2029

Affected areas

Nationwide

Timeline

  1. Initiated
    Mar 13, 2025
  2. Published
    Apr 9, 2025
  3. Terminated
    Jun 11, 2025
Recall number
F-0684-2025
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.