RecallRadar
ModerateReported November 12, 2025

AquaStar Raw Peeled Tail-on Shrimp Skewers

Recalled by Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Product image for 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.
Product image via Open Food Facts. It may show general packaging and not the exact recalled lot — always confirm using the codes below.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. has recalled AquaStar Raw Peeled Tail-on Shrimp Skewers, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 12, 2025 and was initiated on September 20, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers AquaStar Raw Peeled Tail-on Shrimp Skewers, with approximately 5220 cases (8/1.25lbs. bags) affected. The company behind the recall is Admiralty Island Fisheries Inc dba AquaStar (USA) Corp., based in Seattle, WA. The FDA describes the product as: “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.”

Why was AquaStar Raw Peeled Tail-on Shrimp Skewers recalled?

According to the FDA, the stated reason for the recall is: “Shrimp may be contaminated with Cesium-137 (Cs-137).”

What should you do?

If you think you may have bought AquaStar Raw Peeled Tail-on Shrimp Skewers, compare it against the product description and identifying codes (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…) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. or your local health authority.

About this recall

This recall was distributed in WA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Who this recall affects

This recall matters to anyone who bought AquaStar Raw Peeled Tail-on Shrimp Skewers. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.

Distribution listed in the notice: Nationwide..

How to check whether you have it

On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.

Compare what you find against the identifying details in this recall: 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

What to do if you already bought it

Do not eat the product, even if it looks and smells normal — contamination is usually invisible.

Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.

If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. or your local health department.

Full recall details

Status
Ongoing
Date reported
November 12, 2025
Recall started
September 20, 2025
Distributed in
WA
What was recalled
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.
Why it was recalled (as stated by the FDA)
Shrimp may be contaminated with Cesium-137 (Cs-137).
How to identify the affected product
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
Amount recalled
5220 cases (8/1.25lbs. bags)

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was AquaStar Raw Peeled Tail-on Shrimp Skewers recalled?+

According to the FDA: Shrimp may be contaminated with Cesium-137 (Cs-137).

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have AquaStar Raw Peeled Tail-on Shrimp Skewers?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record →

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0159-2026. Information last synced from the FDA on July 27, 2026.

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