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. 1,060 recalls have been distributed to West Virginia in the last 12 months.
Showing 7001–7020 of 48,376 recalls
Recalled Item: MIXED FRUIT BURST 6/10 OZ Packaged in clamshell containers. Recalled by TGD...
The Issue: Potential Salmonella Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FRUIT TRAY W/DIP 3/5 LB Recalled by TGD Cuts, LLC Due to Potential...
The Issue: Potential Salmonella Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MIX FRUIT ALOHA BOWL 3/48 OZ Packaged in clamshell container. Recalled by...
The Issue: Potential Salmonella Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Magnum XXL 9800 Recalled by Meta Herbal Due to Undeclared Active
The Issue: Marketed without an approved NDA/ANDA: Magnum XXL found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIXED FRUIT SPEARS 6/16 OZ. Packaged in clamshell containers. Recalled by...
The Issue: Potential Salmonella Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: External Drainage System Collection Bag Recalled by Natus Medical...
The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYNXGRIP 6F/7F Recalled by Cordis US Corp Due to Cordis became aware that...
The Issue: Cordis became aware that the label for the carton box containing 10 units is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CareEvent Recalled by Philips North America Due to Push notifications...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Packaged Recalled by AtriCure, Inc. Due to AtriCure has identified certain...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Patient Information Center iX Recalled by Philips North America Due to...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYNXGRIP 5F Recalled by Cordis US Corp Due to Cordis became aware that the...
The Issue: Cordis became aware that the label for the carton box containing 10 units is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDS 3 CSF External Drainage System Recalled by Natus Medical Incorporated...
The Issue: Sterility assurance cannot be guaranteed for external drainage systems due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryo Module Accessories Domestic CMA-OUS Recalled by AtriCure, Inc. Due to...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Mobile...
The Issue: Mobile x-ray system can report and deliver a lower post-exposure mAs value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack Recalled...
The Issue: Affected lots may experience increased calibration failures or an increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY Recalled by Acumed LLC Due to...
The Issue: Due to potential breakage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B...
The Issue: The following was missing from the Contraindications Statement: The AVAPS-AE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captus 4000e Thyroid Uptake Systems- Intended to be used by Recalled by...
The Issue: Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.