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. 1,655 recalls have been distributed to West Virginia in the last 12 months.
Showing 44781–44800 of 48,376 recalls
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Product...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
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: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System (product code 6802783) Product Usage:...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Short...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 mm Flared Instrument Cannulae for use with Recalled by Intuitive...
The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 mm Instrument Cannulae for use with the Recalled by Intuitive...
The Issue: Intuitive Surgical is implementing a voluntary Field Action to implement a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHO¿ Assay Software (OAS) Server Recalled by Ortho-Clinical Diagnostics...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...
The Issue: Alphatec Spine initiated this medical device recall for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Multiple studies were missing at a customer location that never made it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...
The Issue: Product did not reach expected sterility assurance level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...
The Issue: Siemens has discovered through product monitoring a potential malfunction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -ENDOPATH ETS-Flex Articulating Endoscopic Linear Cutter Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Glenosphere orientation guide Product Usage: The glenosphere...
The Issue: The Glenosphere Orientation Guide Instrument Used with the Delta XTEND...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...
The Issue: ConMed was notified by the contract manufacturer that their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Relieva Flex Sinus Guide Catheter (Green) Tip Shape: F-70 Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.