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. 2,473 recalls have been distributed to West Virginia in the last 12 months.
Showing 14961–14980 of 27,884 recalls
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Hemi-Artery Recalled by CryoLife, Inc. Due to The...
The Issue: The conduit length and branch length of a SG Pulmonary Hemi-Artery were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec CentriMag Motor Recalled by Thoratec Switzerland GMBH Due to...
The Issue: Reports of circulatory support system motor stopping. Motor stop can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...
The Issue: Product may not meet the internal manufacturing shaft subassembly burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...
The Issue: Increased risk of false positive results for Proteus when the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm 400CE Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm...
The Issue: Potential for membrane (control panel) switch errors leading to an inability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P...
The Issue: Small hole at the end of the syringe is impeding suction of liquid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of...
The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Omega System Recalled by Alpha Omega Engineering Due to If cables are...
The Issue: If cables are improperly connected, current may reach high charge density,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software Correction: Software errors that may result in incorrect 4D CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colpo-Pneumo Occluder Recalled by CooperSurgical, Inc. Due to The seal of...
The Issue: The seal of the sterile pouch may be compromised, thereby increasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor System Elastic Stays (Part 3314-lG Recalled by CooperSurgical,...
The Issue: There is a possibility that the seal of the sterile pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashland(TM) Box Film Ball Cube II EBT3 Recalled by Accuray Incorporated Due...
The Issue: the Ball Cube II phantom calibration film was not manufactured within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 8000i Patient Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solar 9500 Information Monitoring System is used to monitor physiologic...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 5000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dash 4000 Patient Monitoring System is used to monitor physiologic Recalled...
The Issue: The patient monitors may simultaneously restart as designed if all are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.