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 27181–27200 of 27,884 recalls
Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...
The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...
The Issue: The recall was initiated because Carefusion has identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...
The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...
The Issue: Following a single customer complaint that incorrect INR values were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...
The Issue: Hitachi discovered a software error with a feature called Multi-Planar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...
The Issue: Multiple issues were identified with the GE Centricity PACS-IW system that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...
The Issue: Speaker Failure. If the speaker fails and an event occurs which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...
The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware through complaints of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...
The Issue: This letter is to notify you that several of our sterile screw products are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Rover Waste Management System Recalled by Stryker Instruments Div....
The Issue: Stryker has received two reports of serious injury as a result of tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 1 Silver Rover Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker has received two reports of serious injury as a result of tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 1 Gold Rover (120 Vand 230V ) Waste Management Recalled by Stryker...
The Issue: Stryker has received two reports of serious injury as a result of tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.