Welch Allyn, Inc. 901056Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Spot LXi Vital Signs Device with SureTemp Plus Thermometry, SureBP Non-invasive Blood Pressure, Pulse Rate, MAP, BMI Calculation, 50-Reading Memory, Connectivity Ready; 100-240 V, 50-60 Hz AC, Lithium Ion (#105632) Battery; IEC Plug Type-B · 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 00732094003673), received between May 5, 2023 and May 5, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical Shorting” (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
- Electrical Shorting1
- Flare or Flash1
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.
MalfunctionMay 5, 2023Electrical Shorting; Flare or Flash; Electrical Shorting; Flare or Flash
CUSTOMER REPORTED POWER SUPPLY HAD A SHORT. THE POWER CORD FLASHED AND NOW NO LONGER WORKS. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16875831 ↗
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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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