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 9241–9260 of 27,884 recalls
Recalled Item: EPIQ Ultrasound Systems Recalled by Philips Ultrasound Inc Due to Ultrasound...
The Issue: Ultrasound system control panel arm swivel lock could fail, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxA 5000 (DxA Automation System Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that sample carriers (w or w/o samples) within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB Recalled by Cordis Corporation...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL Recalled by Cordis Corporation...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SUPER TORQUE MB 5F PIG Recalled by Cordis Corporation Due to Cordis...
The Issue: Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...
The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH 360 GEN2 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM Recalled by...
The Issue: There is a potential mislabeling of the OAD crown sizes: 1.50mm Sold Crown...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MERITMEDICAL Prelude Short Sheath Introducer Recalled by Merit Medical...
The Issue: There is a potential that a package sheath contains an incorrect dilator.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CritiCool Recalled by Belmont Instrument Corporation Due to Premature pump...
The Issue: Premature pump failure may lead to the device displaying a HALT 4 error,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent...
The Issue: If the device is exposed to fluid ingress and is used before the cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden NKV-550 Ventilator Recalled by NIHON KOHDEN ORANGEMED, INC Due...
The Issue: Potential defective gas inlet pressure regulator within ventilator which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator US PG Recalled by Angiodynamics, Inc. Due to Specific...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solero Generator PG Recalled by Angiodynamics, Inc. Due to Specific serial...
The Issue: Specific serial numbers of the Solero MTA Generator require servicing to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label:...
The Issue: Due to product complaints received for false negative results (dropouts)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.