Welch Allyn, Inc. 901053Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn SureTemp Plus 692 Wall-Mount Electronic Thermometer with 4-6 Second Oral, 10-13 Second Rectal and Pediatric Axillary, and 12-15 Second Adult Axillary Temperature Readings in Fahrenheit or Celsius; Interchangeable Oral Probe Well, Oral Probe with 4.0 ft/1.2 m Cord, Last Temperature Recall, 60-Second Pulse/Respiration Timer, Backlit Display with Electronic ID, Anti-Theft Security System; 3 Alkaline AA Batteries; Multiple Language · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00732094028942), received between May 1, 2024 and Jan 10, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
- Excessive Heating1
Patient problems
- Cough1
- Hemoptysis1
- No Clinical Signs, Symptoms or Conditions1
- Sore Throat1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 10, 2025Excessive Heating; Excessive Heating
CUSTOMER REPORTED PROBE WAS HOT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF#: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21127846 ↗InjuryMay 1, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT DURING THE USE OF THE SURETEMP THERMOMETER THE DISPOSABLE TEMPERATURE PROBE COVER USED WITH THE THERMOMETER REMAINED IN THE PATIENT¿S THROAT AND WAS NOT REMOVED UNTIL THE FOLLOWING DAY. IT WAS ALSO REPORTED THAT DURING THIS EVENT, THE DOCTOR HAD UNDERTAKEN AN ORAL TEMPERATURE CHECK USING THE SAID DEVICE. THE PROBE COVER WAS NOT FULLY CONNECTED TO THIS PROBE, WHICH REQUIRES THE PLASTIC SHEATH TO BE FULLY COVERING THE PROBE AND ON CONNECTION A NOISE CAN BE HEARD AND FELT INDICATING THAT THE PROBE IS IN PLACE. REGRETTABLY THIS ACTION DID NOT RESULT. THIS INCIDENT WAS CAPTURED UNDER HILLROM COMPLAINT REF # (B)(4).
Patient problems: Cough; Hemoptysis; Sore Throat
MAUDE report 19221477 ↗
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- Temperature Probes Esophageal/Rectal Temperature ProbePhilips Medical Systems Hsg · Thermometer, electronic, clinical1 recall1 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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