Home › Carefusion Corporation › AirLife
AirLife
Carefusion Corporation · Model RESNKBT01A · UDI-DI 10885403184536
OGG
Prescription
0
510(k) clearances
751
Adverse events (3 deaths)
2
Recalls
31
Facilities
Description
Airlife™ MM10 SVN Kit, 6" Tube, Elbow with Port, T Adapter
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-13 | Medline Industries, LP | Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, |
| 2014-09-03 | Teleflex Medical | Possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.