Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,547 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,547 in last 12 months

Showing 57815800 of 27,462 recalls

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: Centurion 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 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: Legion 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· Medtronic Neurosurgery

Recalled Item: Medtronic Duet External Drainage and Monitoring system Recalled by Medtronic...

The Issue: Product labeling contains incorrect expiration date

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 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: Constellation Procedure Pak Recalled by Alcon Research, LTD. Due to Reports...

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 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· 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