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Eliachar Laryngeal Stent
HOOD, E BENSON LABORATORIES INC · Model ELL-3000 · UDI-DI 00815347023328
FWN
Prescription
1
510(k) clearances
9
Adverse events
1
Recalls
3
Facilities
Description
Eliachar Laryngeal Stent
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-04-22 | Alveolus, 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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Get your free API keyRead the docsData 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.