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. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 25881–25900 of 48,376 recalls
Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...
The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...
The Issue: Products have been packaged with the wrong Trocar length type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...
The Issue: Final quality control testing was not completed before the devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal Recalled by...
The Issue: Subpotent Drug: The product has failed to maintain its label claim of coal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clocortolone Pivalate Cream Recalled by Dr. Reddy's Laboratories, Inc. Due...
The Issue: Failed Stability Specifications:Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin Acetate Recalled by American Pharmaceutical Ingredients LLC Due...
The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin USP Recalled by American Pharmaceutical Ingredients LLC Due to...
The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...
The Issue: Products labeled for distribution outside the United States may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Optisite Arterial Perfusion Cannula Recalled by SPS...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.