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. 2,537 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,537 in last 12 months

Showing 54415460 of 48,376 recalls

Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: KNEE SCOPE Procedure tray Catalog Number: COKN48L Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND DRAPING SJH-Procedure Kit Catalog Number: SJHD67F Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE - 247546 Procedure tray Catalog Number: BFTK01Z Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: KNEE ARTHROSCOPY-Procedure Kit Catalog Number: QPKA35A Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: KNEE ARTHROSCOPY-Procedure Kit Catalog Number: SLAR14G Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND PACK-Procedure Kit Catalog Number: WEHD16C Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TPK ANTERIOR HIP PACK 176483-Procedure Kit Catalog Number: TPAH21E Recalled...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: ARTHROSCOPY SUP JOI PACK Procedure tray Catalog Number: BPAS17C Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: ARTHROSCOPY WOLFSON PACK BHS Procedure tray Catalog Number: BPAR65A Recalled...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: HAND PACK-Procedure Kit Catalog Number: WEHD16B Recalled by American...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF Recalled by...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· Medtronic Neuromodulation

Recalled Item: A610 Clinician Programmer (CP) Software Application (app) with the following...

The Issue: Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· Hamilton Medical AG

Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...

The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2024· NxStage Medical Inc

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical Inc Due to The...

The Issue: The smaller chamber of the two chamber bag is bursting when nurses are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate...

The Issue: Kit assigned an extended expiration date of 24-Jul-2025 during release. The...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2024· Applied Medical Technology Inc

Recalled Item: AMT Initial Placement Dilator Set. Used to place gastrostomy devices....

The Issue: Devices were labelled with the incorrect guidewire labelling.

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

Class II — Potential Health HazardOngoing