Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,666 recalls have been distributed to Minnesota in the last 12 months.
Showing 5321–5340 of 29,186 recalls
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.
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: 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 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: 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 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: 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: 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 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 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: 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: Merit Pursue Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon...
The Issue: Certain factory settings for the device were incorrectly described in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Cricothyrotomy Field Kit with Instruments Recalled by Sarnova HC,...
The Issue: It was determined that the Endotracheal Tube Holder included in certain kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.