Welch Allyn, Inc. 901058 (REF 75CT-B)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Connex Spot Monitor with SureBP Non-invasive Blood Pressure, Covidien SpO2, SureTemp Plus Thermometer · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00732094209518), received between Nov 22, 2024 and Sep 9, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fire” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Mar 21, 2025Class IIOpen, Classified
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Z-1563-2025 · Root cause: Device Design · Recall details · FDA record ↗
Most reported problems
Device problems
- Fire2
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.
MalfunctionSep 9, 2026Fire
A customer contacted Technical Service to report that a Power Management Stand caught fire. The process step during which this occurred was unknown. There was no patient injury or death reported with this event.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50684343 ↗MalfunctionNov 22, 2024Fire; Fire
THE CUSTOMER REPORTED THE CSM/APM UNIT STARTED 'POPPING' IN A PATIENT ROOM THEN THE PATIENT SMELLED ELECTRICAL BURNING SMELL, COMING FROM A VITALS DEVICE. A NURSE THEN WHEELED THE DEVICE OUT OF THE ROOM AND DOWN THE HALL TO A SAFE PLACE WHEN THE DEVICE BURST INTO FLAMES. THERE WAS NO ADVERSE EVENT REPORTED. THIS INCIDENT WAS CAPTURED UNDER COMPLAINT REF # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20757574 ↗
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- Welch Allyn, Inc. 901058Welch Allyn, Inc. · MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS)2 recalls5 reports
- Welch Allyn, Inc. 901060Welch Allyn, Inc. · MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS)2 recalls3 reports
- Welch Allyn, Inc. 901060Welch Allyn, Inc. · MONITOR,PHYSIOLOGICAL,PATIENT(WITHOUT ARRHYTHMIA DETECTION OR ALARMS)2 recalls2 reports
- McKesson Cardiology Hemo 14.0Change Healthcare Canada Company · Monitor,Physiological,Patient(Without Arrhythmia Detection Or Alarms)2 recalls2 deaths2 reports
- Change Healthcare Cardiology Hemo 14.2Change Healthcare Canada Company · Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)2 recalls1 death1 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 · each recall links to the FDA recall notice
- 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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