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. 2,959 recalls have been distributed to Illinois in the last 12 months.
Showing 641–660 of 55,304 recalls
Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter has determined that, due to a potential communication issue,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prairie Farms Fat Free Milk Recalled by Prairie Farms Dairy Due to Product...
The Issue: Product may contain food-grade cleaning agents
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...
The Issue: Butyrate tube cracks during actuation, rendering product unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Sensor UDI-DI code: 00357599818005 The Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599844011 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599843014 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 3 Plus Sensor UDI-DI code: 00357599819002 Recalled by Abbott...
The Issue: Due to a manufacturing process issue that may cause carbon build up in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: For certain customers, the Change Summary review option ceases to operate as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Vapor 2000. Unheated Recalled by Draeger, Inc. Due to A certain...
The Issue: A certain component of affected devices was not delivered within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: Software issue only allows Concentration Limits to be defined to one digit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to...
The Issue: Ophthalmic procedure packs may have incomplete seals affecting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Vapor 3000. Unheated Recalled by Draeger, Inc. Due to A certain...
The Issue: A certain component of affected devices was not delivered within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOSURE HA SCREW Recalled by Smith & Nephew, Inc. Due to Removal of affected...
The Issue: Removal of affected lot of screws due to labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S. Typhi/Para Typhi A Antigen Recalled by Changchun Wancheng Bio-Electron...
The Issue: Test strips and other tests including for near-patient testing, that require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Male Fertility Sperm Test for Home Use (Cassette) Recalled by Changchun...
The Issue: Test strips and other tests including for near-patient testing, that require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exploro Highly Sensitive Male Fertility / Sperm Concentration Test Recalled...
The Issue: Test strips and other tests including for near-patient testing, that require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.