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. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 31701–31720 of 46,762 recalls
Recalled Item: Norian Drillable Inject 5 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norian Drillable Inject 10 CC-Sterile Recalled by Synthes (USA) Products LLC...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of unexpired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: tabcin NOCHE Recalled by Profarma Distributors LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1% Clotrimazol cream Recalled by Profarma Distributors LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: aloe SPORT liniment TOPICAL ANALGESIC 8 fl oz. tube Recalled by The Aloe...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VERMOX Tablets 500 mg Recalled by Profarma Distributors LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: tabcin ACTIVE M.R. Capsules Recalled by Profarma Distributors LLC Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VERMOX Tablets 100 mg Recalled by Profarma Distributors LLC Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Whole Foods Market Korean BBQ Sauce NET WT 12 OZ Recalled by Whole Foods...
The Issue: Undeclared peanut and coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Recalled by...
The Issue: Product potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Coppertone SUNSCREEN LOTION Recalled by Bayer Health Care LLC Due to...
The Issue: Labeling; Product Contains Undeclared API (Oxybenzone)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tazorac (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tazorac (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...
The Issue: Failed Content Uniformity Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromocriptine Mesylate Capsules USP Recalled by Zydus Pharmaceuticals USA...
The Issue: Failed impurities/degradation specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Revolution CT The system is intended for head Recalled by GE Healthcare,...
The Issue: GEHC has become aware of a potential safety issue in the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products AFP Reagent Pack Recalled by ORTHO-CLINICAL...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed that specific lots of VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal...
The Issue: The device was found to have bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ariol is an automated scanning microscope and image analysis system....
The Issue: An issue during the manufacturing process caused systems to have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System 83 Plus Recalled by Custom Ultrasonics, Inc. Due to To warn...
The Issue: To warn customers that Custom Ultrasonics, Inc. System 83 Plus AERs should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Theratronics cabinet x-ray systems intended for use in the Recalled by...
The Issue: It was discovered that both the new device and the predicate device failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.