Welch Allyn, Inc. 901137 (REF SCNODE-BAA-CNXFX)Recalls & reported problems
Welch Allyn, Inc. · ENG. 110V 32SL 608MHz W MONITORS · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00732094307900), received between Nov 25, 2021 and Nov 25, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Intermittent Communication Failure” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Intermittent Communication Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 25, 2021Intermittent Communication Failure; Intermittent Communication Failure
THE CUSTOMER REPORTED THAT THE NETWORK CONNECTION FROM THE COMPUTERS AT THE SURVEYOR STATION TO THE SWITCH IN THE SERVER ROOM IS GOING OUT INTERMITTENTLY. IT HAS HAPPENED FOR BOTH 16 CHANNEL SYSTEMS AT DIFFERENT TIMES. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12874495 ↗
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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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