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. 2,521 recalls have been distributed to West Virginia in the last 12 months.
Showing 10081–10100 of 27,884 recalls
Recalled Item: NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...
The Issue: Due to not having the full complement of biological assessments for all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...
The Issue: Due to complaints of adverse events potentially related to biological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...
The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...
The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...
The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...
The Issue: The tube holder can separate from the barrier that secures the device to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Operating Table System Recalled by Getinge Group Logistics America, LLC Due...
The Issue: There is a potential for hydraulic leakage at the inclination function to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Recalled by Howmedica Osteonics Corp. Due to Stryker has...
The Issue: Stryker has discovered that the internal profile of the Triathlon Tritanium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...
The Issue: There is a potential that hand control units may cause the tabletop to slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.