MIDAS REX LEGEND 8TD158Recalls & reported problems
Medtronic Powered Surgical Solutions · TOOL 8TD158 LEGND 8CM 1.5MMX8MM TWST DRL · Class 2
All models of MIDAS REX LEGEND (37)
Data updated Oct 16, 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 00763000462437), received between Mar 24, 2023 and May 2, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 2, 2023Fracture; Fracture
IT WAS REPORTED THAT DURING NEUROSURGERY THE DRILL WAS BROKEN AND IT WAS IMPOSSIBLE TO FIND THE PIECE. NO PATIENT IMPACT REPORTED. ON FOLLOW UP IT WAS THAT THERE WAS NO PATIENT OR STAFF IMPACT AND THERE WAS A DELAY IN THE PROCEDURE FOR FIVE MINUTES TO CHANGE THE BURR. IT WAS ALSO REPORTED THAT A COMPUTED TOMOGRAPHY SCAN WAS PERFORMED TO CONFIRM THAT THERE WERE NO FRAGMENTS LEFT INSIDE THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16851718 ↗MalfunctionMar 24, 2023Fracture; Fracture
IT WAS REPORTED THAT THE DRILL BROKE DURING THE OPERATION. NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16608676 ↗
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 · TerminatedMedtronic Midas Rex Dissecting Tool Legend 10 cm 4mm BA DIAM. Intended for use in neurosurgery.
- Z-0321-2016 · Oct 21, 2015 · TerminatedTool 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 · TerminatedMedtronic 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 · TerminatedMedtronic 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 · TerminatedMedtronic 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 · TerminatedMedtronic 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 · TerminatedMedtronic Midas Rex Legend High Speed Pneumatic System
- Z-0213-05 · Nov 3, 2004 · TerminatedMedtronic 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 · TerminatedLegend Lubricant System (Legend Gold, Gold Touch and Platinum motors and Legend Lubricant/Diffuser cartridge)
Other MOTOR, DRILL, PNEUMATIC devices
- NA 05.001.080Synthes GmbH · MOTOR, DRILL, PNEUMATIC432 reports
- NA CSR60Synthes GmbH · MOTOR, DRILL, PNEUMATIC221 reports
- Midas Rex® AF02Medtronic Powered Surgical Solutions · MOTOR, DRILL, PNEUMATIC163 reports
- Maestro Air 5407-200-000Stryker Corporation · MOTOR, DRILL, PNEUMATIC112 reports
- Maestro 5400210060Stryker Corporation · MOTOR, DRILL, PNEUMATIC95 reports
- MIDAS REX™ AF02Medtronic Powered Surgical Solutions · MOTOR, DRILL, PNEUMATIC91 reports
- CORE, Maestro 5400200000Stryker Corporation · MOTOR, DRILL, PNEUMATIC75 reports
- Maestro Air 5407-200-00HStryker Corporation · MOTOR, DRILL, PNEUMATIC56 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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