Chicken of the Sea; Thai Union Recall: Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.

🇺🇸 United States

1. February 4, 2025 - Recall initiated
2. March 19, 2025 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0611-2025

Event ID

96258

Status

Ongoing

Classification

Class II

Company

Chicken of the Sea; Thai Union

Product description

Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48000 13265 UPC# 48000 63267 Product is packaged in several different configurations. shrink wrapped 4- 5 ounce can pack. flat of 24- 5 ounce individual cans. Shrink wrapped 6- 7 ounce can pack.

Quantity

14,147 cases total

Reason

Product's easy-pull lid was not secured properly and may cause the product to become adulterated with the hazard clostridium botulinum.

Recall initiation date

February 4, 2025

Report date

March 19, 2025

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Product was distributed nationwide.

UPC, lot, and code information

Best By dates: 12/13/2027; 1/13/2028; 01/17/2028; 01/21/2028; 01/23/2028; 01/24/2028; 01/27/2028 Lots: S84N D1N; S84N D2M; S84N 41M; S84N 42M; S84N 42N; S84N 43N; S84N D1L; S84N D3L; S84N D1D; S84N D3D; S84N D2D

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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 96258 with 9 other product entries in Public Health Trace.

Responsible company: Chicken of the Sea; Thai Union

Other recalls from Chicken of the Sea; Thai Union

Where this information comes from

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

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

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 "Ongoing." 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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