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. 2,302 recalls have been distributed to West Virginia in the last 12 months.
Showing 40201–40220 of 48,376 recalls
Recalled Item: Hitachi Echelon Oval MRI system is a diagnostic imaging device Recalled by...
The Issue: The Gradient Coil was found to have a failure mode that allowed it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco The Monaco system is used to make treatment plans Recalled by Elekta,...
The Issue: Incorrect Delivery of Composite VMAT Fields - When DICOM is exporting an arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics RESTORATION Acetabular Augment System Recalled...
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...
The Issue: Lumenis initiated a field-correction for the Array Laser Link",...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...
The Issue: Potential issues with the ProVue driver have been identified which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED). For use in general traumatology....
The Issue: The affected Small Electric Drive (SED) may operate solely in reverse mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAM Junctional Tourniquet (SJT) Auxiliary Recalled by Sam Medical Products...
The Issue: SAM Junctional Tourniquet (SJT) Auxiliary strap, model SJT 102 and SJT 112,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ HbA1c Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: In March, Siemens Healthcare Diagnostics issued an Urgent Medical Device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...
The Issue: Defective Container: Product leaks when inverted.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...
The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McCormick Ground Oregano in 0.75 oz plastic bottle. NUMBER: Recalled by...
The Issue: Retail sample of ground oregano tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...
The Issue: An internal finding identified the presence of pinholes/cuts in some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...
The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...
The Issue: Water may leak into the center gas lumen of the Patient Circuit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.