Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. Recall: Shrimp may be contaminated with Cesium-137 (Cs-137).

🇺🇸 United States

1. September 20, 2025 - Recall initiated
2. November 12, 2025 - Reported by source

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0159-2026

Event ID

97667

Status

Ongoing

Classification

Class II

Company

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product description

AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside.

Quantity

5220 cases (8/1.25lbs. bags)

Reason

Shrimp may be contaminated with Cesium-137 (Cs-137).

Recall initiation date

September 20, 2025

Report date

November 12, 2025

Classification date

Not published in this source record

Termination date

Not terminated as of this source record

Distribution pattern

Nationwide.

UPC, lot, and code information

UPC 731149390010; Lot code 10662 5127 10, Best If Used By: 11 07 2027 Lot code 10662 5128 11, Best If Used By: 11 08 2027 Lot code 10662 5133 11, Best If Used By: 11 13 2027 Lot code 10662 5135 10, Best If Used By: 11 15 2027

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

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 97667 with 8 other product entries in Public Health Trace.

Responsible company: Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Other recalls from Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

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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