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. 2,890 recalls have been distributed to Illinois in the last 12 months.
Showing 11101–11120 of 30,032 recalls
Recalled Item: IceSeed" Prostate Cryoablation Kit Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" i-Thaw" Prostate Cryoablation Kit Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceRod" 1.5 MRI 90¿ Cryoablation Needle¿ Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IcePearl" 2.1 CX Prostate Cryoablation Kit Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed" 1.5¿ MRI 90¿ Cryoablation Needle ¿ Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSphere" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) Recalled by Becton...
The Issue: BD has confirmed the presence of blood on the cannulas of the BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bransist Safire Recalled by Shimadzu Medical Systems Due to The firm has...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinias Recalled by Shimadzu Medical Systems Due to The firm has identified...
The Issue: The firm has identified a problem with the control software for the celling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product...
The Issue: Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.