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. 2,480 recalls have been distributed to Alaska in the last 12 months.
Showing 13841–13860 of 46,762 recalls
Recalled Item: The MEDRAD Twist & Go Disposable Syringe 150 mL with Recalled by Bayer...
The Issue: Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Monaco - Product Usage: used to make treatment plans Recalled by...
The Issue: Contour changes can be saved on an unintended image set. In addition, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Bio-Medicus Insertion Kits Recalled by Medtronic Perfusion Systems...
The Issue: There was a label mix-up between two model numbers resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCH Leg Positioning System Recalled by Innovative Orthopedic Technologies,...
The Issue: Due to the holes not being bored to the specific diameter, the locking pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...
The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Foundation Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare Due...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Pack Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenaculum Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrial Biopsy Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Standard IUD Insertion Kit Recalled by Stradis Medical, LLC dba Stradis...
The Issue: Firm unable to confirm that the tenaculum devices were produced in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
The Issue: VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) Recalled by Inpeco S.A. Due to The Firmware (FW) of the...
The Issue: The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the...
The Issue: Software 2.51 and Lower with Installed CO2 Measurement Option, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets USP 100 mg Recalled by Aurobindo Pharma USA Inc....
The Issue: Presence of Foreign Substance: Product complaints received for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kroger 70% Isopropyl Alcohol First Aid Antiseptic 32 FL OZ Recalled by...
The Issue: Labeling: Label Mix-Up.The recall has been initiated after receiving one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TomoHelical and TomoDirect plans in RayStation 6 Recalled by RAYSEARCH...
The Issue: If the dynamic jaw mode is used and an optimization is continued after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee Recalled by...
The Issue: Packaging may include screws that are not intended to be used with the 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.