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. 2,487 recalls have been distributed to Alaska in the last 12 months.
Showing 12961–12980 of 46,762 recalls
Recalled Item: Lexette (halobetasol propionate) Topical Foam Recalled by Mayne Pharma Inc...
The Issue: CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)Traverse Rail Carrier E-System Recalled by Hill-Rom, Inc. Due to Traverse...
The Issue: Traverse rail carriage delivered with non-conforming screws are too short to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1688 Camera Control Unit (CCU) Recalled by Stryker Corporation Due to A...
The Issue: A software defect in the camera control unit (CCU) will cause the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIRRUS HD-OCT Recalled by Carl Zeiss Meditec, Inc. Due to Optic nerve head...
The Issue: Optic nerve head angiography scan to be turned off due to its distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm...
The Issue: Outer labelling (HEMASHIELD GOLD Knitted Microvel Double Velour Bifurcated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUTLER Clear Dip Recalled by Sunstar Americas, Inc. Due to Product lacks...
The Issue: Product lacks premarket clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Inner Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Samaritan PAD Recalled by Physio-Control, Inc. Due to...
The Issue: Semi-automatic defibrillators shipped out by Stryker without battery and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luscient Diagnostics 2nd Generation of COVID-19 Viral Antigen Test For...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra CH Cannulated Hammertoe Mini Instrument Kit-indicated for small bone...
The Issue: During insertion of the middle phalanx implant into bone, the driver may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone...
The Issue: During insertion of the middle phalanx implant into bone, the driver may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LuSys 2nd Generation of COVID-19 Viral Antigen Test For all Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Outer Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.