SureSigns VM1 863264Recalls & reported problems
Philips Medical Systems Hsg · SureSigns VM1 Patient Monitor: Sp02 · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838028906), received between Aug 15, 2019 and Aug 15, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Application Program Freezes or Fails to Launch1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 15, 2019Application Program Freezes or Fails to Launch
THE CUSTOMER CONTACTED THE CUSTOMER CARE SOLUTION CENTER AND REPORTED THAT THE COMPLAINT DEVICE WAS LOCKED IN THE STARTUP MENU. THE DEVICE WAS IN USE ON A PATIENT. THERE WAS NO REPORT OF PATIENT OR USER HARM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8897438 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.