PROvido 000000000010448976Recalls & reported problems
Leica Microsystems (Schweiz) AG · PROvido Stand (Standard) - for Leica surgical operating microscope system: PROvido · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07630003594423), received between Dec 10, 2024 and Mar 25, 2025 — 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.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 25, 2025Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
LEICA MICROSYSTEMS (SCHWEIZ) AG RECEIVED A COMPLAINT FROM GREAT BRITAIN STATING THAT A PROVIDO HAD A LOSS OF ILLUMINATION DURING A SURGICAL PROCEDURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21684964 ↗MalfunctionDec 10, 2024Electrical /Electronic Property Problem; Adverse Event Without Identified Device or Use Problem; Electrical /Electronic Property Problem; Adverse Event Without Identified Device or Use Problem
LEICA MICROSYSTEMS (SCHWEIZ) AG RECEIVED A COMPLAINT FROM TURKEY STATING THAT A PROVIDO HAD A LOSS OF FUNCTION DURING A SURGICAL PROCEDURE. THERE WAS NO PATIENT INJURY. THE FACILITY WHERE THE INCIDENT OCCURRED CANNOT REMEMBER THE DAY OF THE EVENT AND THEREFORE CANNOT PROVIDE AN EXACT DATE. NOVEMBER 26, 2024 IS THE DAY ON WHICH LEICA MICROSYSTEMS (SWITZERLAND) AG BECAME AWARE OF THE INCIDENT. THEREFORE, THIS DATE HAS BEEN ENTERED AS THE DATE OF EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20889753 ↗
Other MICROSCOPE, SURGICAL devices
- M530 Optics Carrier 000000000010448704Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL4 reports
- PROvido 000000000010448950Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL3 reports
- M530 OHX 000000000010448737Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL3 reports
- M525 F20 000000000010448284Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL2 reports
- IMAGE1 PILOT TC014Karl Storz GmbH & Co. KG · MICROSCOPE, SURGICAL2 reports
- M530 Optics Carrier 000000000010448700Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL1 report
- 1788 1788210080Stryker Corporation · Microscope, surgical1 report
- ARveo 000000000010448999Leica Microsystems (Schweiz) AG · MICROSCOPE, SURGICAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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