MIDAS REX® BM110Recalls & reported problems
Medtronic Powered Surgical Solutions · BASE BM110 ELECTRIC BONE MILL ROHS · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00643169999152), received between Sep 4, 2024 and Oct 15, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 reports).
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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component4
- Device Displays Incorrect Message1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 15, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE DEVICE EXHIBITED RATTLING AND A LOOSE PART INSIDE. DURING THE LAST CASE, THE DEVICE COULD BE HEARD RUNNING BUT WAS NOT FUNCTIONING. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23299040 ↗MalfunctionApr 4, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF PARTS DETACHED. NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21775612 ↗MalfunctionSep 17, 2024Detachment of Device or Device Component; Material Integrity Problem; Detachment of Device or Device Component; Material Integrity Problem
REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF CABLE DAMAGED AND DETACHMENT OF COMPONENT. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT. REPAIR IS BEING ESCALATED TO PRODUCT EVENT DUE TO REASON FOR THE RETURN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20234668 ↗MalfunctionSep 4, 2024Device Displays Incorrect Message; Detachment of Device or Device Component; Device Displays Incorrect Message; Detachment of Device or Device Component
REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF ERROR MESSAGE. NO PATIENT IMPACT REPORTED. REPAIR REQUEST ESCALATED TO PRODUCT EVENT ON EVALUATION DUE TO DETACHED COMPONENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20134531 ↗
Other MOTOR, DRILL, ELECTRIC devices
- NA CRANI-A-G1Synthes GmbH · MOTOR, DRILL, ELECTRIC1 recall358 reports
- NA QD8Synthes GmbH · MOTOR, DRILL, ELECTRIC386 reports
- NA QD11-G1Synthes GmbH · MOTOR, DRILL, ELECTRIC312 reports
- Midas Rex EM200Medtronic Powered Surgical Solutions · MOTOR, DRILL, ELECTRIC254 reports
- MIDAS REX MR8 EM800Medtronic Powered Surgical Solutions · MOTOR, DRILL, ELECTRIC186 reports
- Midas Rex MR8 EM800Medtronic Powered Surgical Solutions · MOTOR, DRILL, ELECTRIC158 reports
- NA SHORT-G1Synthes GmbH · MOTOR, DRILL, ELECTRIC134 reports
- Midas Rex® EM200Medtronic Powered Surgical Solutions · MOTOR, DRILL, ELECTRIC123 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.