Midas Rex PM700Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00763000096779), received between Apr 23, 2025 and Jun 17, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (2 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 17, 2026Naturally Worn

  IT WAS REPORTED THAT THE MOTOR WITH THE REPORT OF WORN. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT HOSE DAMAGE WERE FOUND DURING EVALUATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25531351 ↗
• MalfunctionJul 22, 2025Difficult to Insert; Loss of Power; Difficult to Insert; Loss of Power

  REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF LOSS OF POWER. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22569033 ↗
• MalfunctionApr 23, 2025Difficult to Insert; Noise, Audible; Difficult to Insert; Noise, Audible

  REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF NOISE AND DIFFICULTY WITH ASSEMBLY. IT WAS REPORTED THERE WAS NO PATIENT INVO LVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21892769 ↗