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. 2,883 recalls have been distributed to Illinois in the last 12 months.
Showing 12021–12040 of 30,032 recalls
Recalled Item: CMExpress Microbore Set Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset with Needleless Adaptor Recalled by CME America, LLC Due...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Needleless Y Site Microbore Set Recalled by CME America, LLC Due...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Set Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset w/ Non-Vented Spike Connector Recalled by CME America,...
The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...
The Issue: During internal testing execution of the next generation of Integrated Power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell Vantage Stereotactic System Recalled by Elekta Instrument AB Due to...
The Issue: The locking mechanism at the interface of the Instrument Carrier and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expansion Control Overlay Recalled by EHOB, Inc. Due to QC inspection...
The Issue: QC inspection observed that a portion of the lot may have been contaminated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.