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. 1,655 recalls have been distributed to West Virginia in the last 12 months.
Showing 46421–46440 of 48,376 recalls
Recalled Item: West Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150...
The Issue: The firm recalled due to higher reactivity with some samples in the effected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moexipril HCl Tablets 7.5mg Recalled by Paddock Laboratories, LLC Due to...
The Issue: Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Canadian Product: Kellogg's Mini Wheats Recalled by Kellogg Company Due to...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Frosted Mini Wheats Recalled by Kellogg Company Due to This...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: American Vines band Natural Vines Black Soft Licorice Twists Recalled by...
The Issue: Firm's internal sampling of the product found elevated levels of lead in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Mini Wheats Recalled by Kellogg Company Due to This voluntary...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kellogg's Variety and Assortment Packs containing Frosted/ Unfrosted Mini...
The Issue: This voluntary recall is initiated due to the possible presence of fragments...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...
The Issue: Broken screw insertor hardness was measured and found to be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical, Inc. has identified a potential comingling of components where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...
The Issue: A product complaint was received where a size 20 screw was labeled as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Extended Brilliance Workspace (EBW) Recalled by...
The Issue: Incorrect values may be displayed. Philips is issuing a software update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.