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.

48,376 total recalls
2,563 in last 12 months

Showing 15611580 of 27,884 recalls

Medical DeviceMay 22, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....

The Issue: Devices contain potentially out-of-specification levels of endotoxins and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Extended Tip Applicator Recalled by Integra LifeSciences Corp....

The Issue: Devices contain potentially out-of-specification levels of endotoxins and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2025· Jewel Precision Sheet Metal & Machining Co, Inc.

Recalled Item: Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog...

The Issue: The Instructions for Use do not match the 510(k) FDA cleared indications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Product: Atellica CH Diluent - CONS 2 x 1.5L Recalled by Siemens Healthcare...

The Issue: Contamination of the diluent by sodium hypochlorite (NaOCl) which may impact...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Extended Tip Applicator 8CM Recalled by Integra LifeSciences Corp....

The Issue: Devices contain potentially out-of-specification levels of endotoxins and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 22, 2025· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...

The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2025· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to Investigation determined that...

The Issue: Investigation determined that one lot of the T2 Greater Trochanter Nail...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Winged Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: BD Insyte Autoguard Shielded IV Catheter Recalled by Becton Dickinson...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· BIGFOOT BIOMEDICAL

Recalled Item: Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen...

The Issue: Due to a software/firmware issue diabetes management system may provide a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Jolife AB

Recalled Item: LUCAS 2 Recalled by Jolife AB Due to Due to demonstration units of chest...

The Issue: Due to demonstration units of chest compression system being provided to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Becton Dickinson Infusion Therapy Systems, Inc.

Recalled Item: Recalled by Becton Dickinson Infusion Therapy Systems, Inc. Due to Due to...

The Issue: Due to customer complaints, there is the possibility that catheter needle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2025· Covidien

Recalled Item: Newport HT70 Ventilator Recalled by Covidien Due to Ventilator Printed...

The Issue: Ventilator Printed Circuit Board Assembly may have two separate capacitors...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2025· Onkos Surgical, Inc.

Recalled Item: My3D Personalized Solutions Humeral Cup Recalled by Onkos Surgical, Inc. Due...

The Issue: Required inspections were not performed on finished product prior to release...

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

Class II — Potential Health HazardOngoing