Class IIOngoingZ-0876-2026
Microbiologics Inc recalls KWIK-STIK
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Microbiologics IncMNDec 10, 2025
Recalls in Minnesota
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 49–60 of 233 recalls
Class IIOngoingZ-0726-2026
Medtronic, Inc. recalls Aurora EV-ICD and Clinical EV-ICD
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.
Medtronic, Inc.MNDec 10, 2025
Class IIOngoingZ-0574-2026
Sterilmed, Inc. recalls Brand Name: Sterilmed Reprocessed Imaging Catheter Product Name: ACUSON
Affected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead to severe adverse events such as infection, vascular injury or embolism…
Sterilmed, Inc.MNNov 26, 2025
Class IIOngoingZ-0573-2026
Sterilmed, Inc. recalls Brand Name: ACUSON
Affected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead to severe adverse events such as infection, vascular injury or embolism…
Sterilmed, Inc.MNNov 26, 2025
Class IIOngoingZ-0539-2026
Medtronic Perfusion Systems recalls Medtronic HR-ACT (High Range Activated Clotting Time Cartridges)
Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.
Medtronic Perfusion Sy…MNNov 26, 2025
Class IIOngoingZ-0509-2026
Medtronic Perfusion Systems recalls MC3 VitalFlow Console
As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation.…
Medtronic Perfusion Sy…MNNov 26, 2025
Class IIOngoingZ-0487-2026
Medtronic Perfusion Systems recalls Affinity NT Oxygenator
Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas transfer rates that did not meet performance requirements.
Medtronic Perfusion Sy…MNNov 19, 2025
Class IIOngoingZ-0429-2026
Beckman Coulter, Inc. recalls Beckman Coulter UniCel DxI 800
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leadi…
Beckman Coulter, Inc.MNNov 12, 2025
Class IIOngoingZ-0428-2026
Beckman Coulter, Inc. recalls Beckman Coulter UniCel DxI 600
An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leadi…
Beckman Coulter, Inc.MNNov 12, 2025
Class IOngoingZ-0164-2026
IMPRIS Imaging Inc recalls IMRIS Operating Suite
There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite.…
IMPRIS Imaging IncMNNov 5, 2025
Class IOngoingZ-0163-2026
IMPRIS Imaging Inc recalls IMRIS Operating Suite
There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite.…
IMPRIS Imaging IncMNNov 5, 2025
Class IOngoingZ-0162-2026
IMPRIS Imaging Inc recalls IMRIS Operating Suite
There is a potential safety issue associated with the magnet venting paths of the Siemens 3 Tesla MRI system within your IMRIS Operating Suite.…
IMPRIS Imaging IncMNNov 5, 2025