Midas Rex AVA09Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000084974), received between Jun 28, 2021 and Jun 28, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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.

• InjuryJun 28, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT THE SECURE RING TO LOCK THE DRILL BIT WAS TOO TIGHT TO TURN. IT WAS REPORTED THAT THERE WAS A 100-MINUTE PROCEDURE DELAY. NO PATIENT IMPACT REPORTED. IT WAS ALSO REPORTED THAT THE DEVICE WILL NOT BE RETURNED. ON FOLLOW-UP, IT WAS REPORTED THAT THE PATIENT HAD A PROLONGED EXPOSURE TO ANESTHESIA DUE TO THE DELAY, HOWEVER, IT WAS CONFIRMED THAT THERE WAS NO PATIENT IMPACT. IT WAS ALSO REPORTED THAT AN ADDITIONAL ACTION OF EXCESSIVE TURNING OF THE LOCK RING WAS PERFORMED.

  Patient problems: Chemical Exposure

  MAUDE report 12076784 ↗