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. 1,087 recalls have been distributed to Alaska in the last 12 months.
Showing 1261–1280 of 46,762 recalls
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...
The Issue: Due to complaints of increased resistance when advancing the dilator within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNSitu Bipolar Hip System Recalled by Theken Companies LLC Due to Downstream...
The Issue: Downstream recall for RES 97605, BioPro femoral components. Product failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-H190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.