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. 2,550 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,550 in last 12 months

Showing 22612280 of 46,762 recalls

DrugMay 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2025· Cardinal Health 200, LLC

Recalled Item: SCD Comfort Knee Length Small Recalled by Cardinal Health 200, LLC Due to...

The Issue: Incorrect software logic may cause frequent E1 errors (system high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Cardinal Health 200, LLC

Recalled Item: Kendall SCD Blended Comfort Sleeves Knee Length Small - For Recalled by...

The Issue: Incorrect software logic may cause frequent E1 errors (system high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Cardinal Health 200, LLC

Recalled Item: Kendall SCD Comfort Sleeves Knee Length Small Recalled by Cardinal Health...

The Issue: Incorrect software logic may cause frequent E1 errors (system high...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Belmont Instrument LLC

Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...

The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Evolution Upgrade 3.0T Recalled by Philips North America Llc...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 3.0T CX Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T CX Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: MR 7700 Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition X Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for 3.0T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition X Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Elition S Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to Ingenia Elition X Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia Ambition S Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Evolution Upgrade 1.5T Recalled by Philips North America Llc...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for XR and 3.0T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: SmartPath to dStream for 1.5T Recalled by Philips North...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing