MIDAS REX™ ASMCRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000084929), received between Apr 1, 2025 and Apr 1, 2025 — classified as 1 malfunction.

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.

• MalfunctionApr 1, 2025Overheating of Device; Detachment of Device or Device Component; Naturally Worn; Overheating of Device; Detachment of Device or Device Component; Naturally Worn

  IT WAS REPORTED THAT THE PORTION OF THE ATTACHMENT CLOSEST TO THE TIP BECAME LOOSE AND SLID DOWN CUTTING TOOL DURING USE . IT WAS ALSO REPORTED THAT CUTTING TOOL AND ATTACHMENT BECAME HOT AND ATTACHMENT HAD BEEN DISMANTLED AND IN MULTIPLE PIECES. ADDITIONAL INFORMATION REGARDING THE PATIENT IMPACT WAS BEING FOLLOWED UP FROM THE FACILITY. ON FOLLOW-UP IT WAS REPORTED THAT THERE WERE NO PATIENT OR STAFF IMPACT. THERE WAS NO DEVICE FRAGMENT IN THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21737967 ↗