Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,873 recalls have been distributed to New York in the last 12 months.
Showing 3841–3860 of 55,896 recalls
Recalled Item: Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 50 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Regular Strength Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.