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. 2,393 recalls have been distributed to West Virginia in the last 12 months.
Showing 22661–22680 of 27,884 recalls
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...
The Issue: Suboptimal routing of the cable may result in increased wear over time....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...
The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...
The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...
The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...
The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...
The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...
The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...
The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...
The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: While servicing a unit at a customer site, a field engineer discovered a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....
The Issue: Potential for fracture of the tip of the product. The fractured tip is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...
The Issue: A configuration update needs to be done on TactiSys to appropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.