Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,771 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,771 in last 12 months

Showing 59415960 of 29,154 recalls

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
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