Home › KATALYST SURGICAL LLC › 23ga Awh Brilliant Chandelier
23ga Awh Brilliant Chandelier
KATALYST SURGICAL LLC · Model V2105-23V · UDI-DI 10840096211501
MPA
Prescription
10
510(k) clearances
270
Adverse events
1
Recalls
30
Facilities
Description
23ga Awh Brilliant Chandelier, Short 19ga Needle Illumination Connector
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-05 | Alcon Research LLC | Due to incomplete seals in the pouch which provide the sterile barrier. |
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.