Class IITerminated in FDA datasetRecall initiated Mar 13, 2025

SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz.

Recalling firm: Seabear Company

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 11, 2025.

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Compare the exact product and package details with the label you have.

ProductSeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.
UPC034507070211

FDA code information

64241643ALECH Enjoy by: 6/2028 64241641ALECH Enjoy by: 6/2028 64241661ALECH Enjoy by: 6/2028 64243251ALECH Enjoy by: 11/2028 64243261ALECH Enjoy by: 11/2028 64250222ALECH Enjoy by: 1/2029 64250241ALECH Enjoy by: 1/2029

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Full FDA record and distribution details

Original product description

SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.

Extracted codes and context

TypeCode / valueContext
UPC034507070211kedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.

Original FDA recall reason

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

Recall details

Recall number
F-0685-2025
Event ID
96514
FDA status
Terminated
Initiated
Mar 13, 2025
Reported
Apr 9, 2025
Classified
Apr 1, 2025
Terminated
Jun 11, 2025
Quantity
Alehouse Clam Chowder = 5,368 pouches
Location
Anacortes, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed nationwide

FDA source record · F-0685-2025

Data updated September 16, 2026. View official FDA data ↗

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