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. 1,879 recalls have been distributed to West Virginia in the last 12 months.
Showing 11721–11740 of 27,884 recalls
Recalled Item: Sterile Disposable Connectors ASY Y CONN 1/4 X 1/4 X Recalled by LivaNova...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...
The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...
The Issue: The thermo switches in the three-phase transformer, which normally aid in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...
The Issue: If the C-arm leaves its intended travel path due to a fault within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...
The Issue: This field correction is being initiated to address potentially damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...
The Issue: Signature from the user is necessary to proceed with specific actions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.