Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,553 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,553 in last 12 months

Showing 51815200 of 27,462 recalls

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 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 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· 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 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 Volista Recalled by Getinge Usa Sales Inc Due to A potential for 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 Equipment 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 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: 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· 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
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 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 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