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Composite Kit

WESTMED, INC. · Model 0794 · UDI-DI 00709078003899

OGLKFZCAT Prescription
0
510(k) clearances
13
Adverse events
1
Recalls
15
Facilities

Description

Composite Kit,High Flow Humidifier,Adult Cannula w/25'Tubin

Recalls

DateFirmReason
2011-10-17Vital Signs Devices, a GE Healthcare CompanyPovidone Iodine Pads included in the Vital Signs Broselow Pediatric Emergency Kit may be contaminated with Elizabethkinga meningoseptica.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.