Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,654 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,654 in last 12 months

Showing 80418060 of 29,186 recalls

Medical DeviceJune 10, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 11B Recalled by RAYSEARCH LABORATORIES AB Due to This notice...

The Issue: This notice concerns two issues found related to the display of Linear...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Hemoglobin A1c for use with Architect Recalled by Abbott Laboratories Due to...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve ZELTIQ Vaccum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve+ ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCore ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott

Recalled Item: Abbott TactiCath Sensor Enabled Recalled by Abbott Due to When connected to...

The Issue: When connected to the EnSite Precision Navigation System, an affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome HSI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision Chronic Catheter Recalled by Covidien Llc Due to There...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision HSI Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome H Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome SI Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Mahurkar Chronic Carbothane (Maxid) Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Chronic Catheter Recalled by Covidien Llc Due to There is a...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 8, 2022· Covidien Llc

Recalled Item: Palindrome Precision H Chronic Catheter Recalled by Covidien Llc Due to...

The Issue: There is a potential leaking condition within the hub of specific chronic...

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

Class I — Serious Health HazardOngoing