SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label,
Summary
The FDA issued a Class II for SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 1 by Seabear Company. Reason: Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum..
Details
Source
Food Recall
External ID
F-0685-2025
Action Date
2025-04-09
Status
Terminated
Category
food
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.
Lot/Code Info: 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
Quantity Affected: Alehouse Clam Chowder = 5,368 pouches
Reason for Recall
Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Distribution
Distributed nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-13
Company
Anacortes, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Seabear Company has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Seabear Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Seabear Company have FDA actions?
Seabear Company has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0685-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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