Welch Allyn, Inc. 901058 (REF 73MT-B)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Connex Spot Monitor with SureBP Non-invasive Blood Pressure, Masimo SpO2, SureTemp Plus Thermometer · Class 2
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 00732094210071), received between Sep 21, 2023 and Feb 15, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Sparking” (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
- Sparking2
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.
MalfunctionFeb 15, 2024Sparking; Sparking
THE CUSTOMER REPORTED THE CSM DOES NOT POWER ON OR CHARGE. IT WAS ADDITIONALLY REPORTED THE DEVICE WAS PLUGGED INTO A SURGE PROTECTOR AND DEVICE WAS SPARKING WHERE IT WAS PLUGGED IN UNDER THE DEVICE AND SMELLED OF BURNING. THERE WAS NO ADVERSE EVENT REPORTED. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF (B)(4) .
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18712405 ↗MalfunctionSep 21, 2023Sparking; Sparking
CUSTOMER REPORTED DEVICE HAS VISIBLE CHARRING AND PRODUCED SPARKS WHEN PLUGGED IN. THERE WAS NO INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17787987 ↗
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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
- 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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