Product Recalls in Illinois
Product recalls affecting Illinois — including food, drugs, consumer products, medical devices, and vehicles distributed to Illinois. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,932 recalls have been distributed to Illinois in the last 12 months.
Showing 5481–5500 of 30,032 recalls
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: 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: 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 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: 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: 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 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: Fountain Recalled by Merit Medical Systems, Inc. Due to The sterility of...
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: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
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: Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE...
The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator Recalled...
The Issue: AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.