AirLife™ 2074816-001Recalls & reported problems
AirLife Finland Oy · AirLife™ Infant Skin Temperature Probe, Single Patient Use (Giraffe™, Panda™) · 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 10889483577363), received between Apr 1, 2026 and Apr 1, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Output Problem” (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
- Output Problem1
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.
MalfunctionApr 1, 2026Output Problem
IT WAS REPORTED, THE PROBE WAS NOT WORKING AND GIVING A CODE 22. IT WAS NOTED THAT IT MAY BE A WARMER ISSUE. THERE WAS NO REPORT OF A DELAY IN THERAPY, HARM OR INJURY AS A RESULT OF THIS REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24760864 ↗
Other Incubator, Neonatal devices
- Giraffe OmniBed Carestation CS1Datex-Ohmeda, Inc. · INCUBATOR, NEONATAL2 recalls217 reports
- Giraffe Incubator Carestation CS1Datex-Ohmeda, Inc. · INCUBATOR, NEONATAL1 recall37 reports
- Isolette Infant Incubator, Models C2000 and C2000e MU20500Draeger Medical Systems, Inc. · Incubator, Neonatal7 reports
- Babyleo TN500 2M60000Drägerwerk AG & Co. KGaA · Incubator, Neonatal1 death5 reports
- Isolette® 8000 plus MU20602Draeger Medical Systems, Inc. · Incubator, Neonatal3 reports
- AirLife 2075796-001Carefusion Finland 320 Oy · Incubator, Neonatal2 reports
- Isolette 8000 Infant Incubator MU20600Draeger Medical Systems, Inc. · Incubator, Neonatal2 reports
- Airlife 2075796-001AirLife 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.
How reports and recalls are matched · Editorial policy · Report an error on this page