FDA Device Intelligence
HomeMEDLINE INDUSTRIES, INC. › HUDSON RCI

HUDSON RCI

MEDLINE INDUSTRIES, INC. · Model HUD1750 · UDI-DI 10197344097715

BWF Prescription
10
510(k) clearances
182
Adverse events (4 deaths)
1
Recalls
53
Facilities

Description

SPIROMETER,INCENTIVE,LUNG VOLUME

Recalls

DateFirmReason
2020-12-21Smiths Medical ASD Inc.Shipping box may contain wrong model.

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.