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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

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

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 441–460 of 37661 recalls

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.

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.

Altec Forestry Body (Altec) – Labeling Problem (2025)

Altec Industries, Inc. (Altec) is recalling certain 2023-2025 Aerial Device, 2022-2024 Forestry Body, 2022-2025 Service Body, and 2025 Digger Derrick vehicles. The Gross Axle Weight Rating (GAWR) listed on the vehicle certification label may be incorrect, leading to the vehicle being unintentionally overloaded.

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Moderate

NHTSASep 19, 2025Nationwide• ALTEC

Atorvastatin Tablets 20mg (Ascend) – Dissolution Failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDASep 19, 2025Nationwide• Ascend Laboratories, LLC

Atorvastatin Tablets 10mg (Ascend) – Dissolution Failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDASep 19, 2025Nationwide• Ascend Laboratories, LLC

Atorvastatin Tablets 40mg (Ascend) – Dissolution Failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDASep 19, 2025Nationwide• Ascend Laboratories, LLC

Atorvastatin Tablets 80mg (Ascend) – Dissolution Failure (2025)

Failed Dissolution Specifications

Class IIModerate

FDASep 19, 2025Nationwide• Ascend Laboratories, LLC

DxI 9000 Immunoassay Analyzer (Beckman) – result accuracy issue (2025)

Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of user-specified manual dilution factors when ordering additional tests for samples already "In Progress" using the same "Sample ID number". This can lead to false low or high patient results and potential delays in reporting, risking erroneous diagnoses if undetected.

Moderate

FDASep 19, 2025Nationwide• Beckman Coulter, Inc.

DxC 500i Clinical Analyzer (Beckman) – result accuracy issue (2025)

Moderate

FDASep 19, 2025Nationwide• Beckman Coulter, Inc.

Alinity hq Analyzer (Abbott) – Result Flagging Issue (2025)

Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.

Moderate

FDASep 18, 2025Nationwide• Abbott Laboratories

LOGIQ P9 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

HeartSine Pad-Pak (HeartSine) – Defibrillator Pin Damage (2025)

Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.

Moderate

FDASep 18, 2025Nationwide• HeartSine Technologies Ltd 207 Airport Road West Belfast United Kingdom

Zenith Alpha 2 Thoracic Graft (Cook Medical) – PTFE Coating Risk (2025)

Affected devices may contain PTFE coating scrapings. Scrapings could be released during device deployment, potentially causing intravascular embolization.

Moderate

FDASep 18, 2025AL, AZ, AR +28 more• Cook Medical Incorporated

13-Drawer Dressers (EnHomee) – Tip-Over Hazard (2025)

This recall involves EnHomee Fabric 13-Drawer Dressers. The Fabric 13-Drawer Dressers are 55.12" W x 35.45" H x 11.02" D and come in rustic brown, white, black, and pink.

Very High

CPSCSep 18, 2025Nationwide• Changzhou Jiaxuan Intelligent Furniture Co. Ltd., of China

LOGIQ P10 Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

LOGIQ P10 HD Ultrasound (GE Medical) – Measurement Inaccuracy (2025)

Moderate

FDASep 18, 2025Nationwide• GE Medical Systems, LLC

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.

Moderate

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

Taproom Gourmet Fifth Avenue Mix (Egress) – Undeclared Allergens (2025)

Undeclared Allergen

No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)

Class IIModerate

FDASep 18, 2025CA, CT, FL +3 more• Egress Capital Partners Inc.

Kirkland Signature Ahi Tuna Wasabi Poke – Listeria Contamination (2025)

Listeria

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

Class IHigh

FDASep 18, 2025AL, AK, AR +34 more• Western United Fish Company Inc

Taproom Gourmet Park Mix (Egress) – Undeclared Allergens (2025)

Undeclared Allergen

No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashews, wheat, soy, and sesame)

Class IIModerate

FDASep 18, 2025CA, CT, FL +3 more• Egress Capital Partners Inc.