Midas Rex AD01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000084684), received between Apr 3, 2020 and Apr 3, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Remains Activated” (1 report).

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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 3, 2020Device Remains Activated; Naturally Worn; Physical Resistance/Sticking; Device Remains Activated; Naturally Worn; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING A CRANIOTOMY PROCEDURE, THE ATTACHMENT STOPPED SPINNING CAUSING DURAL TEAR. IT WAS ALSO NOTED THAT THE BEARINGS WERE DAMAGED WHEN CHECKED BY THE TECHNICAL SERVICE. ON FOLLOW UP, IT WAS REPORTED THAT A MICROMAR PERFORATOR WAS USED TOGETHER WITH THE PERFORATOR DRIVER AND IT HAS BEEN DISCARDED BY THE CUSTOMER. ADDITIONAL INFORMATION ABOUT THE EVENT IS BEING FOLLOWED UP FROM THE FACILITY CONTACT PERSON.

  Patient problems: Perforation

  MAUDE report 9920892 ↗