Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,558 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,558 in last 12 months

Showing 52215240 of 27,899 recalls

Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Orchide 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/...

The Issue: The internal diameter of the coaxial cannula may be smaller or larger than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Axillary Insertion Introducer -Introducer(s) are intended for...

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· APN Health LLC

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.

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Luminex Corporation

Recalled Item: Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier) Recalled by Luminex...

The Issue: Potentially defective utility trays in the reagent kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing