Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,724 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,724 in last 12 months

Showing 53215340 of 29,284 recalls

Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet PowerLEDII OR Light System 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 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 Hanaulux HLX3000 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 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 Lucea - Lucea10/40 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 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 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 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.

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

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.

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

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.

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

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.

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

Recalled Item: Maquet PowerLED/HLED and PowerLED300 OR Light Systems Recalled by Getinge...

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 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· 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: 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· 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· 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 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