Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,161 recalls have been distributed to Virginia in the last 12 months.
Showing 1981–2000 of 53,829 recalls
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator Recalled...
The Issue: Potential for the manometer port being blocked rendering the manometer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rizatriptan Benzoate Tablets Recalled by Ascend Laboratories, LLC Due to...
The Issue: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Lidocaine HCL Recalled by Imprimis NJOF, LLC Due to Sub-Potent...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide-Proparacaine-Phenylephrine-Ketorolac Recalled by Imprimis NJOF,...
The Issue: Sub-Potent Drug: Subpotent assay results during stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Tablets 90 mg Recalled by Strides Pharma, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Generations 67 and above of VITROS Ca Slides are experiencing an increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein 2% Ophth Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semaglutide Recalled by Boothwyn Pharmacy LLC Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215....
The Issue: Label is incorrect. The product label indicates that the device contains an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Deep Brain Stimulation Systems Surgical Implant Manual Recalled by...
The Issue: Wire break(s) have occurred in rechargeable deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.