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 29813000 of 27,884 recalls

Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Boston Scientific Corporation

Recalled Item: Boston Scientific AVVIGO+ Multi-Modality Guidance System Recalled by Boston...

The Issue: Boston Scientific has received reports indicating the grid mark overlay on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Stryker Corporation

Recalled Item: 1.2mm Cross Cut Fissure - Intended for use in the cutting Recalled by...

The Issue: May exhibit endotoxin levels greater than 2.15 EU/device, fever and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Luminex Molecular Diagnostics Inc

Recalled Item: NxTAG Respiratory Pathogen Panel +SARS-CoV-2 Recalled by Luminex Molecular...

The Issue: Respiratory pathogen panel may report an elevated rate (7.6% predicted...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2024· Luminex Molecular Diagnostics Inc

Recalled Item: NxTAG Respiratory Pathogen Panel Recalled by Luminex Molecular Diagnostics...

The Issue: Respiratory pathogen panel may report an elevated rate (7.6% predicted...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· Bard Peripheral Vascular Inc

Recalled Item: The EVSRF catheter is a sterile Recalled by Bard Peripheral Vascular Inc Due...

The Issue: The Venclose" RF Ablation Catheters may have been manufactured with internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline CENTRAL CATHETER INSERTION TRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline TUBAL LIGATION PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Electrosurgical Generator Recalled by Olympus Corporation of the...

The Issue: There was an increase in complaints indicating an occurrence of system error...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand medical procedure convenience kits Recalled by MEDLINE...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline CHEST TUBE INSERTION TRAY ADUL Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: It has been determined that certain Convenience kits that were packaged in...

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

Class II — Potential Health HazardOngoing