Midas Rex PM710Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000096786), received between Mar 21, 2023 and Mar 21, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

• InjuryMar 21, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE HANDPIECE FORCEFULLY DETACHED FROM THE HOSE AND IT WAS REQUIRED TO REPLACE SOME INSTRUMENTS ON THE FIELD FOR STERILITY, RE-GOWN AND RE-GLOVE, AND RE-DRAPE THE PATIENT. IT WAS ALSO REPORTED THAT HEALTHCARE PROFESSIONAL EXPERIENCED RINGING IN HER EAR AND SOME DECREASED HEARING ACUITY.  IT WAS ALSO REPORTED THAT STAFF WAS STRUCK BY HOSE AND EXPERIENCED HAND PAIN. ADDITIONAL INFORMATION REGARDING THE EVENT WAS BEING FOLLOWED-UP.

  Patient problems: No Clinical Signs, Symptoms or Conditions; Pain; Tinnitus

  MAUDE report 16580198 ↗