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. 1,041 recalls have been distributed to West Virginia in the last 12 months.
Showing 11461–11480 of 27,884 recalls
Recalled Item: Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal Recalled by...
The Issue: Removal for a specific lot, lot number 70128207, of Holder HKHZ 19 for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxA 5000 Recalled by Beckman Coulter Biomedical GmbH Due to The DxA 5000...
The Issue: The DxA 5000 instructions for use may be confusing regarding the re-use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Recalled by FHC,...
The Issue: An electrical sub-circuit was not properly connected. Its purpose is to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Migrating Indicator Recalled by Resource Optimization & Innovation...
The Issue: The firm received reports from customer that the Regard Migrating Indicator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...
The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...
The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...
The Issue: During internal testing execution of the next generation of Integrated Power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leksell Vantage Stereotactic System Recalled by Elekta Instrument AB Due to...
The Issue: The locking mechanism at the interface of the Instrument Carrier and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expansion Control Overlay Recalled by EHOB, Inc. Due to QC inspection...
The Issue: QC inspection observed that a portion of the lot may have been contaminated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista one-piece hydrophobic acrylic toric intraocular lens Recalled by...
The Issue: The toric axis marks were misaligned (from the expected position in relation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips M3015A Microstream CO2 Extension Model No. 862393 -used with...
The Issue: Affected M3015A extensions are incompatible with the lntelliVue X3 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACTIV.A.C Therapy System Recalled by KCI USA, INC. Due to The device may...
The Issue: The device may power off without notification to the user resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.