Home › Avanos Medical, Inc. › Halyard
Halyard
Avanos Medical, Inc. · Model 92811 · UDI-DI 10680651928112
1
510(k) clearances
2
Adverse events
1
Recalls
3
Facilities
Description
HALYARD* Endoscope Cleaning Device
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-09-29 | Stryker Endoscopy | Product may not adequately visualize IR light emitted from U- and E- kits due to a manufacturing error. |
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 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.