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 26941–26960 of 27,884 recalls
Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CRW Precision Arc (CRWPRECISE) Recalled by Integra LifeSciences...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory Recalled...
The Issue: There is potential for the sterility of the product to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...
The Issue: Loss of patient data can occur under certain circumstances due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...
The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...
The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...
The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...
The Issue: The seat could break as a result of damage resulting from a seat belt being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....
The Issue: During the manufacturing of the affected lot a manufacturing error has led...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...
The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.