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.

48,376 total recalls
2,473 in last 12 months

Showing 1490114920 of 27,884 recalls

Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO) Recalled by DePuy Orthopaedics,...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Becton Dickinson & Co.

Recalled Item: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Recalled by...

The Issue: The device may not function at the lower end (<15 deg. C) of the labeled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· AS Software, Inc.

Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....

The Issue: Any change made to current ultrasound machine software or hardware upgrades,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Micro-Tech (Nanjing) Co., Ltd.

Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...

The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...

The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· COVIDIEN LLC

Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...

The Issue: Software Update: External USB Drive performance and its impact on Graphic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2018· Beckman Coulter Inc.

Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...

The Issue: Cross contamination may have occurred between wells for the reagent pack. As...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Sterilmed, Inc.

Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...

The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...

The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· BioMerieux SA

Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...

The Issue: Data loggers showed that one shipment to the United States experienced low...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing