Medtronic Xomed recalls

Medtronic Xomed has 25 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 3 Sep 2025. 16 are still ongoing. The most frequent reason is device malfunction.

Total recalls25since 2012
Last 12 months0reported
Class I416% of total
Ongoing16latest 3 Sep 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 4 16%Class II 21 84%Class III 0 0%

Why medtronic xomed is recalled

By year

Ongoing medtronic xomed recalls

16 active

All medtronic xomed recalls, newest first

25 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIIPC Powerease System recalled by Medtronic XomedMedtronic XomedOther25 states
DeviceCLASS IINIM Vital Nerve Monitoring System: Console NIM4CM01 NIM recalledMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IIMedtronic ENT Ultra Round Steel Cutting Bur recalled by Medtronic XomedMedtronic XomedOtherFL
DeviceCLASS IINIM TriVantage EMG Endotracheal Tubes recalled by Medtronic XomedMedtronic XomedOtherFL
DeviceCLASS INIM EMG Endotracheal Tube, Part Numbers: a) recalled by Medtronic XomedMedtronic XomedOtherNationwide
DeviceCLASS INIM Contact EMG Endotracheal Tube, Part Numbers: a) recalledMedtronic XomedOtherNationwide
DeviceCLASS INIM EMG Endotracheal Tube, Part Numbers: a) recalled by Medtronic XomedMedtronic XomedOtherNationwide
DeviceCLASS IINIM Vital Console 4.0 recalled by Medtronic XomedMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IINIM Vital Patient Interface 4.0 recalled by Medtronic XomedMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IISoftware 1898072 IPC upgrade v 2.7.3.0, IPC System: a) Console recalledMedtronic XomedDevice MalfunctionFL
DeviceCLASS IINIM Trivantage EMG Endotracheal Tube recalled by Medtronic XomedMedtronic XomedOtherNationwide
DeviceCLASS IIMedtronic sterile single-use blades that are components recalledMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IIMedtronic sterile single-use blades that are components recalledMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IIMedtronic Sterile single-use blades that are components recalledMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IISoftware 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC recalledMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IILamicel INTL Cervical dilator recalled by Medtronic XomedMedtronic XomedSterilityFL
DeviceCLASS IILamicel INTL recalled by Medtronic XomedMedtronic XomedSterilityFL
DeviceCLASS IILamicel INTL recalled by Medtronic XomedMedtronic XomedSterilityFL
DeviceCLASS IINIM EMG Endotracheal Tube I.D recalled by Medtronic XomedMedtronic XomedPackaging DefectsNationwide
DeviceCLASS IIUniversal Titanium Prosthesis, Round Head recalled by Medtronic XomedMedtronic XomedOtherNationwide
DeviceCLASS IITray Surgical, ENT (various instrument trays) Used recalledMedtronic XomedOtherNationwide
DeviceCLASS IREF 8229705 x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm recalledMedtronic XomedPackaging Defects29 states
DeviceCLASS IIInterfaces subject to recall: Medtronic NIM recalled by Medtronic XomedMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IIInterfaces subject to recall: Medtronic NIM recalled by Medtronic XomedMedtronic XomedDevice MalfunctionNationwide
DeviceCLASS IIInterfaces subject to recall: Medtronic NIM recalled by Medtronic XomedMedtronic XomedDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.