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 22381–22400 of 46,762 recalls
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK FT3 (FT3: Free Triiodothyronine) is designed for IN Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...
The Issue: Potential for fluorescein interference to cause inaccurately elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitros Myoglobin Calibrators Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: A stability issue in the calibrators may cause calibration failures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Variable Pitch Compression Screw Caddy Recalled by Zimmer Biomet,...
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Variable Pitch Compression Tray Base Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....
The Issue: The surgical technique is being updated to caution against misuse due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aprepitant Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Shortfill: Aprepitant capsules 40 mg is being recalled due to customer...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets 5 mg/160 mg Recalled by Teva...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets 5 mg/320 mg Recalled by Teva...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles Recalled...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets 10 mg/160 mg Recalled by Teva...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: FDA...
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.