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. 2,589 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,589 in last 12 months

Showing 1540115420 of 52,120 recalls

Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP IV SET W/UNIVERSAL SPIKE-single-use for use with the Recalled...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 60 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Blood Administration Set with SAFELINE Injection Site-single...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: ET82HP OUTLOOK PUMP EXTENSION SET-single-use for use with the Outlook...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 10 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: V1500HP OUTLOOK PUMP SET 118-single-use for use with the Outlook Recalled by...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP IV SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Add-On Set-single use Recalled by B. Braun Medical, Inc. Due to...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites: single-use for...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Recalled by DePuy...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing