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. 2,563 recalls have been distributed to West Virginia in the last 12 months.
Showing 1261–1280 of 27,884 recalls
Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...
The Issue: Under certain conditions, such as the simultaneous use of the operating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...
The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mensio Workstation (Vascular Fenestrated) software Recalled by PIE Medical...
The Issue: When fenestrated analysis with clock measurements is started in diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum Duo Infusion System Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical identified two sequences of programming events and alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Mini Handle and Blade by Flexicare...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Mini with Pro Miller Blade Size 1.5 Recalled by Flexicare...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Laryngoscope Handle :040-310AU and...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Handle and Blade : 040-331U (Mac 1)...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood/MacConkey Biplate 100/PK Recalled by Remel, Inc Due to Potential...
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strep Selective II Agar Recalled by Remel, Inc Due to Potential Listeria...
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood/EMB Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.