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. 1,984 recalls have been distributed to Illinois in the last 12 months.
Showing 24481–24500 of 30,032 recalls
Recalled Item: Philips IntelliVue TcG10 Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips has discovered that the Instructions for Use (IFU) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...
The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to Stryker Endoscopy is recalling...
The Issue: Stryker Endoscopy is recalling Laparoscopic manual instruments and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.