Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,061 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,061 in last 12 months

Showing 2521–2540 of 46,762 recalls

Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Medtronic Neuromodulation

Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...

The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...

The Issue: The device was delivered with a preassembled Femoral Augment screw that was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Preat Corp

Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...

The Issue: Due to manufacturing issues, abutment products were manufactured with screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2025· Amerisource Health Services LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...

The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 2, 2025· Getinge Disinfection Ab

Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...

The Issue: The frequency inverter is not programmed by supplier according to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2025· Philips North America Llc

Recalled Item: Philips Brilliance CT Big Bore Recalled by Philips North America Llc Due to...

The Issue: Unintended motion issues related to Interventional Control that may lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2025· IBA Dosimetry GmbH

Recalled Item: myQA iON Recalled by IBA Dosimetry GmbH Due to Wrong analysis results can...

The Issue: Wrong analysis results can occur if the user creates two structures with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 1, 2025· TONY'S CHOCOLONELY INC

Recalled Item: Tony's Chocolonely Dark Chocolate Almond Sea Salt Recalled by TONY'S...

The Issue: Contains foreign objects (stones)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 1, 2025· TONY'S CHOCOLONELY INC

Recalled Item: Tony's Chocolonely Everything Bar Recalled by TONY'S CHOCOLONELY INC Due to...

The Issue: Contains foreign objects (stones)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2025· Ultra Clean Systems, Inc.

Recalled Item: Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72...

The Issue: During routine preventative maintenance checks, it was revealed that carbon...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 31, 2025· B. Braun Medical Inc

Recalled Item: 0.9% Sodium chloride Irrigation USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit. Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit. Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2025· AVID Medical, Inc.

Recalled Item: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit Recalled...

The Issue: An issue with a raw material used to coat some surgical needles that may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 31, 2025· Denver Solutions, LLC DBA Leiters Health

Recalled Item: PHENYLephrine HCl in 0.9% Sodium Chloride Recalled by Denver Solutions, LLC...

The Issue: Lack of Assurance of Sterility: Leaking/damaged syringes.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund