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. 2,455 recalls have been distributed to West Virginia in the last 12 months.
Showing 16001–16020 of 48,376 recalls
Recalled Item: Power Injectable CT Port insertion kits - Product Usage: is Recalled by...
The Issue: The 5F Dignity CT Port kits were packaged with the incorrect size port. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm Recalled by...
The Issue: incorrect device is contained in the package. The packaging label indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENROUTE Transcarotid Stent System Recalled by Silk Road Medical Inc Due to...
The Issue: Due to complaints received that the tip/nose cone may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...
The Issue: The external drainage system failed to meet Pyrogen test requirements for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: Incorrect Labeling: Incorrect lot number on secondary packaging
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...
The Issue: The device catheter tip was cut off (no tip) and the product packaging was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...
The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nortriptyline HCl Capsules Recalled by Taro Pharmaceuticals U.S.A., Inc. Due...
The Issue: CGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to...
The Issue: Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended...
The Issue: Potential for false negative diagnosis of gastroparesis. Certain GEBT kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Femoral Sleeves - Product Usage: used primarily in revision...
The Issue: The taper dimensions may be out of specification due to a production issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mephyton (phytonadione) Tablets 5mg Recalled by Bausch Health Companies,...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by American...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The PrisMax System Version II Hemodialysis Delivery System: Automatic...
The Issue: Variability in the performance of the tubing in the ARPS (Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.