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. 2,000 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,000 in last 12 months

Showing 43014320 of 46,762 recalls

Medical DeviceSeptember 3, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Centurion Sterile CirClamp Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Product has been identified as having holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T - For use as a Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Evolution Upgrade 3.0T - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition S - For use as a diagnostic device Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T CX - For use as a diagnostic device Recalled by Philips North...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2024· Philips North America Llc

Recalled Item: Ingenia Elition X- For use as a diagnostic device to Recalled by Philips...

The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...

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

Class II — Potential Health HazardOngoing
FoodSeptember 3, 2024· Blue Tape Sriracha

Recalled Item: Blue Tape Sriracha sauce is condiment Recalled by Blue Tape Sriracha Due to...

The Issue: Acidified product was manufactured by firm without ODA license.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2024· Ascend Laboratories, LLC

Recalled Item: Mycophenolic Acid Delayed-Release Tablets USP Recalled by Ascend...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 3, 2024· Vivier Pharma, Inc.

Recalled Item: Vivier Sheer SPF 30 Mineral With Antioxidants (titanium dioxide 10% Recalled...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mupirocin Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2024· Hammond's Candies Since 1920 II, LLC

Recalled Item: Hammond's Dark Chocolate Filled Mini Waffle Cones Recalled by Hammond's...

The Issue: Undeclared allergen: milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing