InjuryQUQ
KAHOOK DUAL BLADE GLIDE
Received Jan 27, 2026 · Event occurred Dec 30, 2025
Report 1000125279-2026-00001 · MDR key 24188644
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Hyphema
Narrative
Description of Event or Problem
DR. PERFORMED A KDB GLIDE AND PATIENT INCURRED MILD, CONTROLLED HYPHEMA (B)(6) 2025.
Additional Manufacturer Narrative
THE DEVICE HISTORY RECORD (DHR) COULD NOT BE REVIEWED, AS NO SPECIFIC SERIAL OR LOT INFORMATION WAS AVAILABLE. THE PRODUCT WAS MANUFACTURED, TESTED, AND RELEASED IN ACCORDANCE WITH VALIDATED PROCEDURES. AS THE DEVICE IS NOT AVAILABLE FOR RETURN, NO DEVICE MALFUNCTION COULD BE CONFIRMED.