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Laryngeal Umbrella Keel

HOOD, E BENSON LABORATORIES INC · Model LK-16 · UDI-DI 00815347023366

FWN Prescription
1
510(k) clearances
9
Adverse events
1
Recalls
3
Facilities

Description

E. Benson Hood Laboratories Umbrella Keel

Recalls

DateFirmReason
2004-04-22Alveolus, Inc.The tracheal stent may collapse resulting in blockage of the air passage because the stents were not properly coated with the polyurethane material to the very end of the stent.

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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.