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. 2,372 recalls have been distributed to West Virginia in the last 12 months.
Showing 24321–24340 of 27,884 recalls
Recalled Item: The Synthes Hohmann Retractor Recalled by Synthes, Inc. Due to The Synthes...
The Issue: The Synthes Hohmann Retractor was mis-etched on the product and package as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS BUN UREA NITROGEN For the In vitro quantitative determination Recalled...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS URIC ACID For the In vitro quantitative determination of Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AST For the In vitro quantitative determination of AST Recalled by AMS...
The Issue: Marketing the devices outside 510(k) requirements
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Thermedx Fluid Management System is designed to provide irrigation...
The Issue: A vendor changed the manufacturing process of a component used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BencoDental tartar & stain remover ultrasonic cleaning solution Product...
The Issue: As the result of a complaint to Heraeus Kulzer's customer service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to Potential safety...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis Systems Product usage: Artis zee is a family Recalled by Siemens...
The Issue: Certain units of the AXIOM Artis Systems are using a flat detector cooling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMP X-alt Acetabular Liner This acetabular liner is intended for Recalled by...
The Issue: Packaging error -- two different types and sizes of acetabular liners used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia and Infinia Hawkeye Nuclear Medicine Systems. For...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger PS500 Power Supply Unit of the Infinity ACS Workstation Recalled by...
The Issue: The battery capacity of the optional PS500 Power Supply Unit of the Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product...
The Issue: Baxter Healthcare Corporation has issued an Urgent Device Correction for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: Potential safety issue related to unintended radial detector motion, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pega Medical Inc. Recalled by Pega Medical Inc. Due to The Male Components...
The Issue: The Male Components in this lot are made of material with lower strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Home and OnSite (HS1) automated external defibrillators...
The Issue: Philips is recalling HeartStart Home and OnSite (HS1) automated external...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Everest 20cc Inflation Device Recalled by Medtronic Vascular Due...
The Issue: Incorrect master label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 5.0mm Variable Locking Screw This device is part of Recalled by...
The Issue: Labeling correction: The package insert in one 5.0mm Variable Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Brand Name(s): Alere Triage¿ TOX+MTD Drug Screen Recalled by Alere...
The Issue: Alere San Diego, Inc. is initiating a recall of the Alere Triage¿ TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisherbrand Sterile Swabs Recalled by Fisher Scientific Co Due to A customer...
The Issue: A customer reported the presence of an organism in a lot of Calcium Alginate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux B200 Flux Dialyzers Recalled by Fresenius Medical Care Holdings,...
The Issue: Dialysate Port Leak During Priming of the Dialyzers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.