AirLife 2075796-001 (UDI 10885403260759)Recalls & reported problems
Carefusion Finland 320 Oy · Infant Skin Temperature Probe, Reusable (Giraffe™, Panda™) · 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 10885403260759), received between Aug 7, 2020 and Jan 31, 2023 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Temperature Problem” (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.
Most reported problems
Device problems
- Temperature Problem2
Patient problems
- Burn(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 31, 2023Temperature Problem; Temperature Problem
THE CUSTOMER REPORTED TO VYAIRE MEDICAL THAT THE 2075796-001 GIRAFFE REUSABLE SKIN TEMP PROBE AIR TEMPERATURE IS SHOWING BELOW 30 DEG. PROBLEM OCCURRED ON PATIENT USE AS INFORMED BY THE CUSTOMER NO INJURY REPORTED TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16275548 ↗InjuryAug 7, 2020Temperature Problem; Temperature Problem
THE CUSTOMER REPORTED THAT A PATIENT SUFFERED A BURN INJURY INVOLVING THE AIRLIFE INFANT SKIN TEMPERATURE PROBE, AND MEDICAL INTERVENTION WAS REQUIRED TO TREAT THE WOUND.
Patient problems: Burn(s)
MAUDE report 10382894 ↗
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- Babyleo TN500 2M60000Drägerwerk AG & Co. KGaA · Incubator, Neonatal1 death5 reports
- Isolette® 8000 plus MU20602Draeger Medical Systems, Inc. · Incubator, Neonatal3 reports
- Isolette 8000 Infant Incubator MU20600Draeger Medical Systems, Inc. · Incubator, Neonatal2 reports
- Airlife 2075796-001AirLife Finland Oy · INCUBATOR, NEONATAL1 report
- AirLife™ 2074816-001AirLife Finland Oy · Incubator, Neonatal1 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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