Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,380 recalls have been distributed to West Virginia in the last 12 months.
Showing 22721–22740 of 27,884 recalls
Recalled Item: Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and...
The Issue: HORIBA Medical is informing all HORIBA Medical Lite DM customers using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...
The Issue: KCI has received reports that, in a small number of cases, the CelluTome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...
The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...
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: ECG Out Cable Recalled by Philips Electronics North America Corporation Due...
The Issue: When a Philips monitor/defibrillator is receiving an ECG signal from an...
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.