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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 22021–22040 of 46,762 recalls
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...
The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl CD capsules Recalled by Valeant Pharmaceuticals North America...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...
The Issue: The vertical dimensions of screw-hole position in some standalone cages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ephedrine Sulfate Recalled by US Compounding Inc Due to Lack of assurance of...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Lupin Pharmaceuticals Inc....
The Issue: Failed Impurities/Degradation Specifications: OOS results observed in any...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Smart Disclosure System Recalled by Spacelabs...
The Issue: Several reports were received that patient records were printed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kii Fios First Entry Recalled by Applied Medical Resources Corp Due to The...
The Issue: The product may not have met sterility requirements . Use of a non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.