Olympus WM-NP2 (UDI 15019778004105)Recalls & reported problems
Keymed (Medical & Industrial Equipment) Limited · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 15019778004105), received between Mar 30, 2021 and Apr 15, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Break” (4 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
- Break4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 15, 2024Break; Break
IT WAS OBSERVED THAT DURING THE DEVICE EVALUATION, THE WORKSTATION SET 3 EXHIBITED A BROKEN CASTOR ON THE HOUSING. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19105088 ↗MalfunctionJun 6, 2023Break; Break
IT WAS REPORTED TO OLYMPUS BY A BIOMEDICAL ENGINEER THAT A WM-NP2 WORKSTATION¿S CASTOR BROKE OFF. IT IS UNKNOWN WHEN THE REPORTED ISSUE WAS FOUND. IT IS UNKNOWN WHEN THE REPORTED ISSUE WAS FOUND. THE DEVICE WILL NOT BE RETURNED DUE TO THE ISSUE BEING RESOLVED. THERE WAS NO PATIENT INJURY OR ADVERSE EVENT REPORTED TO OLYMPUS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17075069 ↗MalfunctionJun 10, 2021Break; Break
THE SERVICE CENTER WAS INFORMED THAT THE WORKSTATION SET HAD A BROKEN WHEEL MALFUNCTION AS THE BOLT SNAPPED IN HALF DURING AN UNSPECIFIED PROCEDURE. NO PATIENT OR USER INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11980138 ↗MalfunctionMar 30, 2021Break; Break
THE SERVICE CENTER WAS INFORMED THAT THE CASTOR WHEEL BROKE OFF THE WORKSTATION. THERE WAS NO USER/PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11587947 ↗
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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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