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. 2,554 recalls have been distributed to Alaska in the last 12 months.
Showing 41–60 of 46,762 recalls
Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...
The Issue: Due to complaints and investigations stating that alarms from the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units...
The Issue: Potential for rubber fragment detachment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Teva...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Why Not Natural Moringa Capsules 120 capsule bottle marked with Recalled by...
The Issue: Potential to be contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE Recalled by Medline...
The Issue: Fabric may experience premature delamination when using included laundering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP. Product Code: 0046-0011. Recalled by Abiomed, Inc. Due to...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist. Product Code: 1000323. Recalled by...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist. Product Code: 0046-0035. Recalled by Abiomed,...
The Issue: Differential pressure (dP) sensor in Impella RP devices may malfunction,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029....
The Issue: During the bulk packaging process, some Luer Slip syringes were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARITY II Laser System Recalled by Lutronic Corporation Due to Reports of...
The Issue: Reports of devices sparking/popping and potentially burning patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESTRADIOL Recalled by F.H. INVESTMENTS, Inc. (dba Asteria Health) Due to...
The Issue: Presence of Foreign substance - potential presence of metal particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trazodone Hydrochloride Recalled by Granules Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRADIOL Recalled by F.H. INVESTMENTS, Inc. (dba Asteria Health) Due to...
The Issue: Presence of Foreign substance - potential presence of metal particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Recalled by F.H. INVESTMENTS, Inc. (dba Asteria Health) Due to...
The Issue: Presence of Foreign substance - potential presence of metal particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.