M525 F20 000000000010448284Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630003551907), received between Jan 15, 2025 and Jan 23, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 23, 2026Electrical /Electronic Property Problem

  LEICA MICROSYSTEMS (SCHWEIZ) AG RECEIVED A COMPLAINT FROM ITALY STATING THAT A M525 F20 HAD A FAILURE OF THE MAIN AND BACKUP ILLUMINATION DURING SURGERY. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24158402 ↗
• MalfunctionJan 15, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  LEICA MICROSYSTEMS (SCHWEIZ) AG RECEIVED A COMPLAINT FROM CHINA STATING THAT AN M525 F20 HAD A LOSS OF ILLUMINATION DURING A SURGICAL PROCEDURE. THERE WAS NO PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21155253 ↗