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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 1841–1860 of 46,762 recalls
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Description/ PYXIS MEDBANK MINI 1FH-1FM/169-137 Recalled by CareFusion 303,...
The Issue: Reports of delayed access to medication in automated dispensing cabinets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein 2% Ophth Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Tablets 90 mg Recalled by Strides Pharma, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide-Proparacaine-Phenylephrine-Ketorolac Recalled by Imprimis NJOF,...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Lidocaine HCL Recalled by Imprimis NJOF, LLC Due to Sub-Potent...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Generations 67 and above of VITROS Ca Slides are experiencing an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.