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. 2,336 recalls have been distributed to West Virginia in the last 12 months.
Showing 33381–33400 of 48,376 recalls
Recalled Item: American Surgical Delicot-J 13 mm x 60 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Cotton Balls-Non-Strung 3/4" : 31-03 Product Usage:...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Policot 1/2" x 2" : 90-29 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Delicot non-xray 5 mm x 8 mm by American Surgical Company...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Delicot 5 mm x 8 mm : Recalled by American Surgical...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Americot Blue 3/8" x 2" : 20-26S Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Surgical Ray-Cot 1/2" x 1.5" : 60-08 Product Recalled by American...
The Issue: Product packaging defective compromising sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...
The Issue: E. CAM and Symbia system with foresight detectors performing gated or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...
The Issue: The firm identified an issue in sample processing when using EZee-Nest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...
The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...
The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...
The Issue: The software did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: If a reader selects Multi-study review prior to the original study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...
The Issue: The fasteners securing the control panel assembly to the base of the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....
The Issue: There is a potential connection issue when powering up the Merge Hemo Record...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...
The Issue: Eye Station images were not importing properly and were imported under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...
The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.