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. 2,530 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,530 in last 12 months

Showing 65816600 of 27,884 recalls

Medical DeviceMarch 27, 2023· Smith & Nephew, Inc.

Recalled Item: JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith &...

The Issue: A mispack occurred during the manufacturing process, resulting in the box...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2023· Richard Wolf GmbH

Recalled Item: FLEX. BIOPSY FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...

The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2023· Richard Wolf GmbH

Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...

The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2023· Richard Wolf GmbH

Recalled Item: FLEX. GRASP. FORCEPS 6.6FR WL 550MM Recalled by Richard Wolf GmbH Due to...

The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2023· Richard Wolf GmbH

Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...

The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2023· Covidien

Recalled Item: Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Recalled by...

The Issue: A manufacturing error, resulted in a less than specified diameter of adult...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 23, 2023· ASO LLC

Recalled Item: WALGREENS BANDAGES Recalled by ASO LLC Due to The adhesive bandage contains...

The Issue: The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Diagnostica Stago, Inc.

Recalled Item: STA Compact Automated Multi-Parametric Analyzer Recalled by Diagnostica...

The Issue: An internal investigation identified a bug in this firmware version,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Diagnostica Stago, Inc.

Recalled Item: STA Compact Max fully automatic clinical analyzer Recalled by Diagnostica...

The Issue: An internal investigation identified a bug in this firmware version,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Diagnostica Stago, Inc.

Recalled Item: STA R Max fully automatic clinical instrument designed to perform Recalled...

The Issue: An internal investigation identified a bug in this firmware version,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number 800706005 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800753005 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 880393003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 11mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880353009 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880473001 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· ROi CPS LLC

Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...

The Issue: The recalling firm was notified by their supplier that the light handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2023· Covidien LP

Recalled Item: VersaOne Reusable Positioning Cannula 12mm Standard Recalled by Covidien LP...

The Issue: There is a manufacturing non-conformance that may result in a metal shaving...

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

Class II — Potential Health HazardOngoing