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. 2,834 recalls have been distributed to New Jersey in the last 12 months.
Showing 5361–5380 of 29,496 recalls
Recalled Item: Maquet G8 / G8E OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Axcel / Axcel + OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux HLX2000 OR Light Systems Recalled by Getinge Usa Sales Inc...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Hanaulux 2006/ 2007 Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet XTen OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Prismalix OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Rolite OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Blueline Series 30/80 OR Light Systems Recalled by Getinge Usa Sales...
The Issue: A potential for a light system to fall in the operating room.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System is designed as a modular system with components Recalled by GE...
The Issue: GE HealthCare has become aware of the potential that incorrect torque has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oscor Intro Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Oscor Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navik 3D v2 Recalled by APN Health LLC Due to IFU update
The Issue: IFU update
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The System is designed as a modular system with components Recalled by GE...
The Issue: GE HealthCare has become aware of the potential that incorrect torque has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed KIT Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oscor Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...
The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.