Midas Rex® PM710Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00613994486257), received between Jun 1, 2017 and Jun 1, 2017 — 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.

• InjuryJun 1, 2017Device Remains Activated; Device Remains Activated

  IT WAS REPORTED THAT THE MOTOR DID NOT STOP SPINNING WHEN THE SURGEON TOOK THE HAND OFF THE HAND CONTROL. THE PATIENT HAD A DURA TEAR, BECAUSE THE MOTOR WOULD NOT STOP SPINNING. ON FOLLOW UP, IT WAS REPORTED THE PATIENT WAS REQUIRED TO STAY OVERNIGHT DUE TO THE CSF LEAK AND FOR MONITORING. THE PATIENT HAS SINCE BEEN DISCHARGED, BUT THE CURRENT CONDITION IS UNKNOWN. THERE WAS NO ADDITIONAL PATIENT INFORMATION AVAILABLE. THE SURGICAL PROCEDURE WAS A LAMINOTOMY (SPINAL SURGERY - NO FUSION). THE INITIAL REPORTER INFORMATION AND PARTIAL CONCOMITANT DEVICE INFORMATION WAS ALSO PROVIDED. ON FURTHER FOLLOW UP WITH THE DOCTOR, IT WAS REPORTED THE PATIENT WAS WELL POSTOPERATIVE. THE DURA LEAK WAS ADDRESSED WITH NO PATCH USED.

  Patient problems: Cerebrospinal Fluid Leakage; Perforation

  MAUDE report 6606343 ↗