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. 2,348 recalls have been distributed to Alaska in the last 12 months.
Showing 26141–26160 of 46,762 recalls
Recalled Item: O-arm¿ O2 interventional fluoroscopic x-ray system Recalled by Medtronic...
The Issue: During servicing of certain internal components of the O-Arm O2 Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Knee...
The Issue: Knee implant components (tibial bearings) are labeled with the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Costco item # 1052939 Recalled by Tai Foong USA Inc Due to Undeclared Egg
The Issue: Royal Asia brand Shrimp Wonton Noodle Soup is recalled due to undeclared egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Birds Eye Baby Sweet Peas Recalled by Pinnacle Food Group, Llc Due to...
The Issue: Product has the potential to be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled...
The Issue: Correction to update sterilizer software to prohibit the use of expired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The...
The Issue: Users manuals not supplied with 4800-00T US Rapid Therapy System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous...
The Issue: A specific lot of the FlexFlowTM Venous Cannula, 200-200, is being recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...
The Issue: There have been reported incidents of fluid leaks at the luer connection....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...
The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Mobius Imaging, LLC Due to If the...
The Issue: If the tilt-drive motor has an intermittent connection or broken encoder or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...
The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...
The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.