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

🇺🇸 United States

1. March 13, 2025 - Recall initiated
2. April 9, 2025 - Reported by source
3. June 11, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0684-2025

Event ID

96514

Status

Terminated

Classification

Class II

Company

Seabear Company

Product description

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.

Quantity

Salmon Chowder = 11,152 pouches

Reason

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

Recall initiation date

March 13, 2025

Report date

April 9, 2025

Classification date

Not published in this source record

Termination date

June 11, 2025

Distribution pattern

Distributed nationwide

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 96514 with 1 other product entry in Public Health Trace.

Responsible company: Seabear Company

Other recalls from Seabear Company

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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