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. 2,521 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,521 in last 12 months

Showing 1006110080 of 27,884 recalls

Medical DeviceFebruary 24, 2021· Arthrex, Inc.

Recalled Item: Drill Bit Recalled by Arthrex, Inc. Due to The color indicator on the...

The Issue: The color indicator on the proximal end of the shaft of the AR-8770-02 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2021· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Philips CT systems are advanced continuous-rotation computed tomography...

The Issue: Philips has internally detected an issue with the actuators used in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2021· Trinity Sterile, Inc.

Recalled Item: Midline Catheter Dressing Change Kit with Statlock - Product Usage: Recalled...

The Issue: Evidence of face masks or other material in the seal in several kits,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 4.5 Recalled by RAYSEARCH LABORATORIES AB Due to For some LINAC...

The Issue: For some LINAC types, merging clinical beams with beams of approximate dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Safe Sheath Ultralite - Vascular Introducer/Catheter...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Smart Port CT-Implantable Port Catalogue #: CT96STSD-VI Recalled by...

The Issue: AngioDynamics, Inc. is recalling a specific batch of AngioDynamics...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· DePuy Orthopaedics, Inc.

Recalled Item: The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee Recalled by...

The Issue: Globally the company is removing 37 lots affected lots for MBT & ATTUNE (S+)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Sirtex Medical Limited

Recalled Item: SIROS D-Vial Prep Set Recalled by Sirtex Medical Limited Due to There is a...

The Issue: There is a potential presence of particulate matter in the D-Vial.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00...

The Issue: BeneVision DMS may intermittently freeze and require a manual reboot after...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· Sunstar Americas, Inc.

Recalled Item: SUNSTAR G.U.M. HYDRAL DRY MOUTH RELIEF On-the-go Oral Spray Recalled by...

The Issue: The product may be contaminated with Burkholderia cepacia

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Smisson-Cartledge Biomedical, LLC

Recalled Item: ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge...

The Issue: Customers are being notified of results from a Toxicological Risk Assessment...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 18, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 4-(Calibrator values for TIBC...

The Issue: Potential total iron-binding capacity (TIBC) results. The VITROS TIBC...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2021· TELEFLEX MEDICAL INC

Recalled Item: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct...

The Issue: Teleflex is voluntarily recalling the products above due to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2021· Vectornate USA Inc

Recalled Item: MedSchenker Smart Transport Medium (STM) System: CULTURE MEDIA Recalled by...

The Issue: Discoloration and turbidity were present in the specified lots of STMs...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2021· Clerio Vision

Recalled Item: EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for Recalled by...

The Issue: Contact lenses may be mislabeled with the incorrect lens power.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2021· CARESTREAM DENTAL, LLC

Recalled Item: Carestream Dental CS 3600 Single Use Normal Tips Recalled by CARESTREAM...

The Issue: The mirror may become detached and fall from the unit

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

Class II — Potential Health HazardOngoing