FDA Device Intelligence
HomeMEDLINE INDUSTRIES, INC. › HUDSON RCI

HUDSON RCI

MEDLINE INDUSTRIES, INC. · Model HUD78001KIT · UDI-DI 10197344010752

OGG Prescription
0
510(k) clearances
723
Adverse events (3 deaths)
2
Recalls
31
Facilities

Description

CIRCUIT, NEO, SING LIMB, HTD,COLUMN

Recalls

DateFirmReason
2026-07-13Medline Industries, LPNeonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke,
2014-09-03Teleflex MedicalPossibility 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 docs
Data 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.