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. 2,508 recalls have been distributed to Alaska in the last 12 months.
Showing 9941–9960 of 46,762 recalls
Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Apotex Corp. Due to Failed...
The Issue: Failed Stability Specifications: Out of specification for weight loss at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...
The Issue: Failed Impurities/Degradations Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alsultan Sweets Betefour 10.5oz (600 grams) Recalled by FALCON IMPORT &...
The Issue: Undeclared cashews, almonds, and pistachios
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alsultan Sweets Mixed Baklava 12.3oz (350 grams) /750 grams Recalled by...
The Issue: Undeclared milk and wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Monitor/ScanWatch Recalled by Withings Due to A software bug eliminated...
The Issue: A software bug eliminated the initial ECG activation and review of the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size...
The Issue: All lots of BIOSTOP G Bioresorbable Cement Restrictor are being removed as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epinephrine (L-Adrenaline) Recalled by Spectrum Laboratory Products, Inc....
The Issue: Discoloration: Product complaints of the repackaged Epinephrine API being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine (L-Adrenaline) Recalled by Spectrum Laboratory Products, Inc....
The Issue: Discoloration: Product complaints of the repackaged Epinephrine API being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ganciclovir for Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Tablets Recalled by Aurolife Pharma, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.