Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,871 recalls have been distributed to Maryland in the last 12 months.
Showing 5341–5360 of 29,093 recalls
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.
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.
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: 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 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.
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.
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: 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: 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.
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 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.
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.
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: 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: 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: 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.