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 8241–8260 of 27,884 recalls
Recalled Item: BF-MP160F: EVIS EXERA Bronchofibervideoscope Recalled by Olympus Corporation...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BF-3C160: EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...
The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...
The Issue: Software error may result in sporadic problems causing scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...
The Issue: Upgraded software version makes an automatic change in laser configuration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson 9vE4 Transducer Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Transducers (component of ultrasound system) may exceed recommended thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...
The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....
The Issue: Software issue resulting in temporary loss of central monitoring functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...
The Issue: The product was distributed without FDA authorization or clearance for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...
The Issue: During the de-installation of an MR system magnet, if all rigging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...
The Issue: Sterility failure of the exterior of the syringe which may impact the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VESSEL SEALER EXTEND Recalled by Intuitive Surgical, Inc. Due to Placing...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.