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Humidifier Nebulizer Kit

FDA product code OGG · Class 2 · Anesthesiology

196

Registered devices

723

Adverse events

2

Recalls

0

510(k) clearances

Devices with this code

HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED AirLife™ — AIRLIFE HUDSON RCI — TELEFLEX INCORPORATED Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.HUDSON RCI — MEDLINE INDUSTRIES, INC.HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED Yirdoc — Qingdao Future Medical Technology Co., Ltd.HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED Yirdoc — Qingdao Future Medical Technology Co., Ltd.HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED AirLife™ — AIRLIFE AirLife — Carefusion Corporation HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — TELEFLEX INCORPORATED HUDSON RCI — MEDLINE INDUSTRIES, INC.

Recent 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 discolorat
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.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.