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. 2,460 recalls have been distributed to West Virginia in the last 12 months.
Showing 15881–15900 of 27,884 recalls
Recalled Item: Quadra Assura MP Recalled by St Jude Medical Inc. Due to The firm is...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Current Recalled by St Jude Medical Inc. Due to The firm is releasing new...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter Recalled by Cook...
The Issue: Incorrect product labeling. Product labeled as 6mm x 2cm balloon are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Promote Quadra Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...
The Issue: The firm is releasing new firmware for high voltage implantable cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...
The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...
The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...
The Issue: Devices inappropriately displayed a low battery indicator determined to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8Fr. Catheter Clamp with Fastener Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peel Away Sheath over Dilator Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Multi-Lumen CVC Kit Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.