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. 2,525 recalls have been distributed to West Virginia in the last 12 months.
Showing 8201–8220 of 27,884 recalls
Recalled Item: Ultrasonic Gastrovideoscope Recalled by Olympus Corporation of the Americas...
The Issue: GF-UC140P-AL5 is no longer a compatible endoscope for reprocessing in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: regard Clinical Packaging...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience kits containing regard IV Start Kits: (1) regard Clinical...
The Issue: A drug kit component was recalled by its manufacturer due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion GBS Assay Cartridges 96 Tests Recalled by Hologic, Inc Due to...
The Issue: Samples, run on a GBS Assay, that have analyte concentrations that are at or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinici X da Vinci Xi Sureform 45 Recalled by Intuitive Surgical, Inc. Due...
The Issue: As a result of complaint data review, it identified tissue pushout events...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LetsGetChecked Blood Sample Collection kit-In vitro diagnostic medical...
The Issue: Users received sample collection kits that were assigned to another user....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEISS miLOOP Lens Fragmentation Device . Used during cataract Recalled by...
The Issue: High friction of the slider can cause the device to stick, or not move as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Separation Technology Creamatocrit Plus Recalled by Stanbio Laboratory, LP...
The Issue: The device was being marketed as an IVD without a 510(k). Therefore,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrisMax System Recalled by Baxter Healthcare Corporation Due to This...
The Issue: This correction is due to software anomalies occurring during use. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M3 RT ADULT-US Model: 32028777 50600...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...
The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...
The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...
The Issue: Due potential misuse of the product, firm is updating warnings and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...
The Issue: System software v1.5.1 has a system software issue related to the Daylight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.