Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,653 recalls have been distributed to New Jersey in the last 12 months.
Showing 25841–25860 of 29,496 recalls
Recalled Item: Amo-O Herbal Stimulator Recalled by Altasource LLC dba Meta Labs LLC Due to...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nice-En-Smooth Berry Burst Recalled by Altasource LLC dba Meta Labs LLC Due...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Recalled by Siemens Medical Solutions Diagnostics Due to There...
The Issue: There is a potential for incorrect results to be reported from processing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hot Ice Recalled by Altasource LLC dba Meta Labs LLC Due to Firm is not...
The Issue: Firm is not registered as a drug manufacturer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...
The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Power Supply is an accessory for the GemStar Recalled by Hospira...
The Issue: The GemStar Infusion pump may not receive direct current (DC) power from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET PLEGIOX Cardioplegia Heat Exchanger The PLEGIOX Cardioplegia Heat...
The Issue: The MAQUET post-marketing vigilance program has identified a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Otto Bock Aerial and Aerial Active Wheelchair Cushions. Material numbers:...
The Issue: Otto Bock is recalling all Aerial and Aerial Active Wheelchair Cushions from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to The connection between...
The Issue: The connection between the beeper subassembly and the pump may fail. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Greatbatch Medical Recalled by Greatbatch Medical Due to Greatbatch Medical...
The Issue: Greatbatch Medical has initiated a global Field Corrective Action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001: Prevena Peel and Place System Kit Product Usage: The Recalled by...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1055US: Prevena Dressing Recalled by KCI USA, INC. Due to Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE1001US: Prevena Peel and Place System Kit (US-ONLY) Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY)...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Battery Powered Driver Recalled by Synthes, Inc. Due to The CMF...
The Issue: The CMF Battery Powered Driver graphic case contains outlines of the Battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2001: Prevena Incision Management Customizable System Box Product Usage:...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRE2055: Prevena Customizable Dressing 5-Pack Product Usage: The Prevena...
The Issue: Prevena Incisional Management System Kit/Dressing Connector - the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select CAP Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Select 3D Arterial Cannulae. Vented Recalled by Medtronic Inc....
The Issue: Medtronic is recalling all models of its Select 3D and Select CAP Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.