Airlife 2075796-001 (UDI 10190752179622)Recalls & reported problems
AirLife Finland Oy · Infant Skin Temperature Probe, Reusable · 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 10190752179622), received between Jun 7, 2022 and Jun 7, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (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
- Overheating of Device1
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.
MalfunctionJun 7, 2022Overheating of Device; Overheating of Device
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE AIRLIFE¿ INFANT SKIN TEMPERATURE PROBE, REUSABLE (GIRAFFE¿, PANDA¿) WARMER WAS OVERHEATING. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT. THE EVENT OCCURRED DURING PRE-USE CHECK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14627341 ↗
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™ 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.
How reports and recalls are matched · Editorial policy · Report an error on this page