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. 2,464 recalls have been distributed to West Virginia in the last 12 months.
Showing 15561–15580 of 27,884 recalls
Recalled Item: Liquid Cardiac Control - Level 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: The device is not suitable for the control of the Troponin T assay due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...
The Issue: The product labels (pouch and carton) for products contain an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...
The Issue: The latest on-site software version may not have been reinstalled at some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...
The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...
The Issue: GE Medical Systems has discovered a small area on the bore surface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The firm has learned that some RayStation/RayPlan users have commissioned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Chamber Temporary External Pacemaker Recalled by Medtronic Inc.,...
The Issue: A subset of Medtronic Model 53401 Single Chamber External Pulse Generators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fx SOLUTIONS CENTERED HEAD CoCr 50x19 Recalled by Fx Solutions Due to Breach...
The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Microsystems products labeled as the following: Leica M320 Microscope...
The Issue: Possible failure of screws which hold the gas spring fixation bracket in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fx SOLUTIONS OFFSET HEAD CoCr 50x20 Recalled by Fx Solutions Due to Breach...
The Issue: Breach in the external blister of certain lots of Humelock Offset Head 50 X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeoMed Enteral Feeding Tubes with Enteral Only Connectors Recalled by Neomed...
The Issue: Potential for the tethered plug on the hub of the NeoMed Enteral Feeding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.