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. 2,437 recalls have been distributed to West Virginia in the last 12 months.
Showing 18761–18780 of 27,884 recalls
Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...
The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...
The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...
The Issue: Disengaged screw head could potentially not be retained in the Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...
The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Recovery of Incorrect Isocenter -operational change
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...
The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens is providing software update version VA50A_SP3 to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...
The Issue: A product issues happens for RF projection images. If user measures on RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Software defect:2D projection of contours in Verity. The defect causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...
The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...
The Issue: Hardware issue that may expose the user to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Hardware issue that may expose the User to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.