Skip to content

Midas Rex® AF01-RRecalls & reported problems

Medtronic Powered Surgical Solutions · ATT AF01-R LEGEND F1 (B-5) 2.4MM REFURB · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00613994422217), received between Oct 26, 2018 and Jan 11, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Puncture/Hole” (1 report).

9 other recalls cover devices cleared under the same FDA submission (K020069); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Material Puncture/Hole1
  • No Apparent Adverse Event1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 11, 2019Material Puncture/Hole; Material Puncture/Hole

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF BURR GUARD WAS BROKEN OFF. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT. REPAIR REQUEST ESCALATED TO A PRODUCT EVENT BASED ON REASON FOR RETURN.

    Patient problems: No Patient Involvement

    MAUDE report 8239264 ↗
  • MalfunctionOct 26, 2018No Apparent Adverse Event; No Apparent Adverse Event

    REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF NOT WORKING PROPERLY. IT WAS REPORTED THAT THERE WAS NO PATIENT IMPACT. UPON DECONTAMINATION, IT WAS DETERMINED THAT FOOT WAS DETACHED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8011105 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K020069. One submission often covers many models, so check the product and lot details in each record.

  • Z-1602-2016 · Apr 8, 2016 · Terminated
    Medtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use in neurosurgery.
  • Z-0321-2016 · Oct 21, 2015 · Terminated
    Tool Legend 16cm 2.4 mm wire pass for Midas Rex Legend Dissecting Tool. Used by surgeons to drill holes.
  • Z-0546-2010 · Nov 30, 2009 · Terminated
    Medtronic Midas Rex Legend Footed Attachment, AF01. Intended for use with all Legend and Legend EHS motors for general surgery including maxillofacial , craniofacial and sternotom
  • Z-2156-2008 · May 30, 2008 · Terminated
    Medtronic Midas Rex Legend tapered dissecting tool, Model F2/8TA23 Medtronic Powered Surgical Solutions, Forth Worth, TX Intended for use in Spinal, Cranial, Orthopedic, General S
  • Z-1574-05 · Sep 1, 2005 · Terminated
    Medtronic Midas Rex Classic, GS and Legend dissecting tools manufactured by Medtronic Inc. Powered Surgical Solutions, 4620 North Beach Street, Fort Worth, tX 76137 USA, Rx only, S
  • Z-1067-05 · Jun 29, 2005 · Terminated
    Medtronic MIDAS REX Legend High Speed Pneumatic System, Gold Touch Motor. Manufactured by Medtronic, Inc. Powered Surgical Solutions, 4620 North Beach Street, Fort Worth, TX 76137
  • Z-0278-05 · Nov 11, 2004 · Terminated
    Medtronic Midas Rex Legend High Speed Pneumatic System
  • Z-0213-05 · Nov 3, 2004 · Terminated
    Medtronic Midas Rex Legend Lubricant/ Diffuser Cartridge Catalog number PA100-A, manufactured by Medtronic Powered Surgical Solutions, Fort Worth, Texas
  • Z-0419-03 · Nov 11, 2002 · Terminated
    Legend Lubricant System (Legend Gold, Gold Touch and Platinum motors and Legend Lubricant/Diffuser cartridge)

Other MOTOR, DRILL, PNEUMATIC devices

All MOTOR, DRILL, PNEUMATIC devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page