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 24181–24200 of 27,884 recalls
Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArjoHuntleigh Contoura C1000 series beds are designed to accommodate...
The Issue: There is a low but existing entrapment risk for a patient being treated on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...
The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended...
The Issue: Injection port of the Set may leak blood/ IV fluids from the septum of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...
The Issue: The footboard of Patient support for stitching can be fixed in upper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...
The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm 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: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS Recalled by...
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: 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: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.