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. 2,550 recalls have been distributed to Alaska in the last 12 months.
Showing 3421–3440 of 46,762 recalls
Recalled Item: Nhan Sam Tuyet Lien Truy Phong Hoan Recalled by Buy-Herbal Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found the products to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FORCE FOREVER 400mg Tablets Recalled by GNMart LLC Due to Marketed without...
The Issue: Marketed without an approved NDA/ANDA. FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dabigatran Etexilate Recalled by Ascend Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dabigatran Etexilate Recalled by Ascend Laboratories, LLC Due to CGMP...
The Issue: CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...
The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...
The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pediatric One-Piece Arterial Cannulae Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Series Angled Tip Arterial Cannula Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist Recalled by Abiomed, Inc. Due to Optical Sensors...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...
The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...
The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biological Recalled by HF Acquisition Co LLC Due to Spore test strip...
The Issue: Spore test strip monitoring system, designed for routine monitoring of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.