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 21412160 of 27,884 recalls

Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: BORN ON ARRIVAL KIT Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: URO ROBOTIC PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL ANGIO PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PPS Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: AV FISTULA Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: THORACIC PACK Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: Beckman Coulter identified that an issue for DxI 9000 tip stocker interface...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis: Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to Sync...

The Issue: Sync timeout may occur between the server and automated dispensing device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: OPEN HEART A PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CV BASIC PUMP PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: MAJOR DIEP Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: SPINE LUMBAR PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: NEURO IR TRAY Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: EAR PACK Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: TOTAL HIP PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· Integra LifeSciences Corp.

Recalled Item: AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to...

The Issue: Possibility for the obturator to break (separate).

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Medical Information Technology, Inc.

Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...

The Issue: Entering multiple keys that trigger input simultaneously may remove data...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...

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

Class II — Potential Health HazardOngoing