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 8081–8100 of 27,884 recalls
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Start-up time for the flow rate range greater than 50 ml/hr, and less than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Ivenix, Inc. Due to Downstream...
The Issue: Downstream occlusion alarm is sometimes immediately followed by a pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper...
The Issue: Part (A-rubber) intended for a different model of gastrointestinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonovideoscope Model CF-H180AL Recalled by Olympus Corporation of the...
The Issue: A (Camera unit) CCD intended for a different model of colonoscope may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to There is the potential that...
The Issue: There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Synergy Washer/Disinfector Recalled by Steris Corporation Due to...
The Issue: The firm identified that when the electrical contactor component in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market Recalled...
The Issue: Firm received 10 complaints of skin barrier delamination issues (e.g. flange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...
The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version...
The Issue: Due to interference with the Live Listen feature of hearing aid or AirPods,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...
The Issue: Product label was printed without the UDI number and warning label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...
The Issue: The warning label was printed with the incorrect weight capacity. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.