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 58415860 of 27,884 recalls

Medical DeviceJune 28, 2023· Alcon Research, LTD.

Recalled Item: Infinity FMS Pak Recalled by Alcon Research, LTD. Due to Reports of patient...

The Issue: Reports of patient injury during use in procedures due to potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Alcon Research, LTD.

Recalled Item: Alcon Custom Pak Recalled by Alcon Research, LTD. Due to Reports of patient...

The Issue: Reports of patient injury during use in procedures due to potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Alcon Research, LTD.

Recalled Item: Phaco Standalone Tips Recalled by Alcon Research, LTD. Due to Reports of...

The Issue: Reports of patient injury during use in procedures due to potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Covidien LP

Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...

The Issue: Catheter center lumen was found to have an occlusion in the tip of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Maquet Cardiovascular, LLC

Recalled Item: ACROBAT SUV Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2023· Maquet Cardiovascular, LLC

Recalled Item: ACCESSRAIL Platform (Standard Blade) Part Number SB-1000 Recalled by Maquet...

The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2023· Maquet Cardiovascular, LLC

Recalled Item: ACROBAT-i Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...

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

Class II — Potential Health HazardOngoing