AirLife™ AH265 (UDI 10889483595909)Recalls & reported problems
Airlife · AirLife™ Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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 16, 2026.
Recalls naming this device
- Apr 10, 2025Open, Classified
Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.
Z-1698-2025 · Root cause: Component design/selection · Recall details · FDA record ↗
Other Anesthesia Breathing Circuit Kit (Adult & Pediatric) devices
- AirLife™ 2K8000Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- AirLife™ 2K8001Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax 1 MP02730Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- AirLife™ AH265Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax HEPA MP17102Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax 3 MP02732Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- Anesthesia Circuit Kit Flex 6 MP02744Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)6 reports
- AirLife™ AH202Airlife · Anesthesia breathing circuit kit (adult & pediatric)5 reports
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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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