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. 2,012 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,012 in last 12 months

Showing 401420 of 48,376 recalls

Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm Recalled...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tornier, Inc

Recalled Item: TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE Recalled by...

The Issue: A specific lot of screws is incorrectly labeled. Screws are labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha.Pro Software applications: syngo.CT Brain Quantification...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: Alphenix INFX-8000F Recalled by Canon Medical System, USA, INC. Due to It...

The Issue: It has been discovered that there is a possibility that the fixing screws of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Boston Scientific Corporation

Recalled Item: *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm...

The Issue: Increased reports of stent deployment and expansion issues. The most common...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical, Inc.

Recalled Item: Tego Connector: Recalled by ICU Medical, Inc. Due to Needle free access...

The Issue: Needle free access device intended as accessory to vascular access used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT...

The Issue: To remove the software applications from certain CT systems as the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Recalled by Imprimis NJOF, LLC Due to Presence of...

The Issue: Presence of particulate matter - Glass like particles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Dexamethasone Moxifloxacin Ketorolac Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2025· Imprimis NJOF, LLC

Recalled Item: Tri-Moxi+¿ (Triamcinolone 9mg/0.6mL Recalled by Imprimis NJOF, LLC Due to...

The Issue: Presence of particulate matter - Glass like particles.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing