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. 2,404 recalls have been distributed to West Virginia in the last 12 months.
Showing 20521–20540 of 27,884 recalls
Recalled Item: Product 8 consists of all products under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 3 consists of all products under product code JDI Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 15 consists of all product code JDI Recalled by Zimmer Manufacturing...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 56 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 42 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 43 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 4 consists of all products under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 16 consists of all product under poduct code: KWY Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be Recalled by...
The Issue: Increased punch height, causing a 0.063 in (1.6 mm) gap between the trial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kopans Breast Lesion Localization Needle The Kopans Breast Lesion...
The Issue: Product potentially exposed to body fluids during processing. Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator. Recalled...
The Issue: NatalCare LX Incubators were manufactured using a defective oval port hinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0...
The Issue: In DS/US proton planning, there is a correction factor used internally to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This...
The Issue: Olympus America Inc is conducting a voluntary removal/corrective action of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API ZYM Bx2 () Product Usage: ZYM B reagent Recalled by BioMerieux SA Due to...
The Issue: Discrepant identification results related to API identification strips....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System: HeartWare Battery Recalled by...
The Issue: Heartware Ventricular Assist System Battery Cell experiencing premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Recalled...
The Issue: Some of the Access ClearVue Prone Breast devices may contain scales that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.