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Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. Recalls

All product recalls associated with Admiralty Island Fisheries Inc dba AquaStar (USA) Corp..

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Recall Summary

Total Recalls

50

Past Year

15

Class I (Serious)

0

Most Recent

Sep 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–20 of 50 recalls

Raw Peeled Shrimp Skewers (AquaStar) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Frozen Raw EZ-Peel White Shrimp (Waterfront Bistro) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Raw Colossal EZ Peel Shrimp (Kroger) – Cesium-137 contamination (2025)

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

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Class II

Moderate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Raw Shrimp Easy Peel Deveined (AquaStar) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Mercado Cooked Peeled Shrimp (Kroger) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Extra Large Easy Peel Shrimp (Publix) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Frozen Raw EZ-Peel White Shrimp (Best Yet) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Large Peeled Shrimp (Publix) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Frozen Raw EZ-Peel White Shrimp (AquaStar) – Cesium-137 contamination (2025)

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

Class IIModerate

FDASep 20, 2025Nationwide• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Airvo 2 (Fisher & Paykel) – Power Disconnection Risk (2025)

When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for less than 120 seconds, which may delay user awareness to reconnect power, which could lead to oxygen desaturation, hypoxia. Disinfection kit user manual updated to include checking the audible alert prior to use on a new patient.

FDASep 18, 2025Nationwide• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

Raw Frozen Shrimp (Beaver Street Fisheries) – cesium contamination (2025)

Product may be contaminated with Cesium-137 (Cs-137)

Class IIModerate

FDAAug 15, 2025AR, FL, IL• Beaver Street Fisheries, Inc.

Breaded Shrimp (AquaStar) – Cesium-137 contamination (2025)

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

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Kroger Cooked Shrimp (AquaStar) – Cesium-137 contamination (2025)

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

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

AquaStar Cocktail Shrimp (Admiralty Island) – Cesium-137 contamination (2025)

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

Class IIModerate

FDAAug 14, 2025AL, AK, AR +27 more• Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Pacific Hemostasis Thromboplastin-D (Fisher Diagnostics) – Incorrect ISI Label (2025)

The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.

FDAMar 6, 2025PA• Fisher Diagnostics

Airvo 3 Respiratory Device (Fisher & Paykel) - High Pressure Oxygen Risk (2024)

Due to a software issue, affected devices that are set up with High Pressure Oxygen (HPO), if the flow alignment alarm occurs, the device will deliver room air only. If this happens, a patient my experience oxygen desaturation that could lead to hypoxia.

FDAAug 7, 2024AZ, CA, CO +26 more• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand: Airvo 2 Humidifier, REF: PT101US, and myAirvo 2 Humidifie...

Humidifier devices, used to deliver high flow respiratory therapy to patients, manufactured before 14 August 2017, have a speaker configuration that may result in distorted, intermittent or inaudible alarm sound levels. In the absence of an audible alarm, if there is an interruption to therapy, a patient may experience oxygen desaturation.

FDAApr 2, 2024Nationwide• Fisher & Paykel Healthcare, Ltd. 15 Maurice Paykel Place East Tamaki Auckland New Zealand

Fisher Wallace Laboratories Inc.: Fisher Wallace Stimulator Models FW-100 and FW-200

If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.

FDAApr 6, 2023Nationwide• Fisher Wallace Laboratories Inc.

Hand Sanitizer (Fisher) - CGMP Manufacturing Issue (2023)

CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary approval, into the market after March 31, 2022.

Class IIModerate

FDAJan 17, 2023Nationwide• Fisher Scientific Co., LLC

Hand Sanitizer (Fisher) - CGMP Manufacturing Issue (2023)

CGMP Deviations: Voluntary recall of all hand sanitizer distributed after March 31, 2022, due to FDA issued guidance to cease placing hand sanitizer product, produced under temporary approval, into the market after March 31, 2022.

Class IIModerate

FDAJan 17, 2023Nationwide• Fisher Scientific Co., LLC