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 25961–25980 of 46,762 recalls
Recalled Item: Meclizine hydrochloride tablets USP Recalled by Jubilant Cadista...
The Issue: Marketed without an approved NDA/ANDA: Bottles were released prior to final...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol Recalled by Dr....
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride Recalled by Pharmedium Services,...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...
The Issue: Report was of an interrupted MR scan after patient complained about acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...
The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...
The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...
The Issue: L3 has determined in airport environments, there have been several cases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...
The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...
The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...
The Issue: Failed dissolution specifications; all lots within expiry are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Tablets Recalled by Amerisource Health Services Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: rHead Recon Stem Implant non-coated Recalled by Howmedica Osteonics Corp....
The Issue: Revision rate identified as higher than other proximal radial head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.