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. 2,473 recalls have been distributed to West Virginia in the last 12 months.
Showing 15021–15040 of 27,884 recalls
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitalBeam Radiotherapy Delivery System Version 2.5 Product Usage: The...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA Circular Stapler with Tri-Staple Technology Recalled by COVIDIEN LLC Due...
The Issue: The firm identified the potential for a device to have an incorrect tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...
The Issue: This correction decision has been made because of a potential failure of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 Product Usage: The DX-D 600 system is a Recalled by Agfa N.V. Due...
The Issue: A supplier for the Agfa system noted a potential for the steel support...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System-For use in the in vitro quantitative Recalled...
The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MassHunter Quantitative Analysis Software Recalled by Agilent Technologies,...
The Issue: When utilizing specific software versions of an LC/MS device, and Batch at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System- (). For use in the in Recalled by...
The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...
The Issue: The firm has become aware that the angled-hole of certain semi-tubular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...
The Issue: The action is being initiated due to potential installation of faulty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 15000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO CENTRIFUGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO 9000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO RACK OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 9000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO INPUT/OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.