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. 2,283 recalls have been distributed to Alaska in the last 12 months.
Showing 41341–41360 of 46,762 recalls
Recalled Item: FEM HD ION (various sizes) Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001 Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Recalled by...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...
The Issue: GE became aware of a potential safety issue due to a system slow down and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...
The Issue: If the couch, with the footrest extension attached, is positioned where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...
The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...
The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...
The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...
The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...
The Issue: A review of complaints identified a trend for drills breaking.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.