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 24221–24240 of 27,884 recalls
Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck Vista Cannula-only Recalled by Teleflex Medical Due to Complaints...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Fixt Suture Braided Polyester Recalled by Teleflex Medical Due to...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIO Recalled by Teleflex Medical Due to The product did not meet minimum...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dekna-lok Recalled by Teleflex Medical Due to The product did not meet...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA...
The Issue: Some 23 kHz Torque Wrenches were incorrectly assembled and contained a 36...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API Listeria (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: API NIH (). ZYM B reagent is used and Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FB Reagent (). FB reagent is an additional test Recalled by BioMerieux SA...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZYM B Reagent (). The ZYM B reagent is Recalled by BioMerieux SA Due to...
The Issue: bioMerieux identified a visual defect and activity issue on the ZYM B...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: A customer reported that after upgrading to software version 3.5.5 from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.