inforMED
MalfunctionGBW

CORE REPOSAL TRUMPET

Received Jan 13, 2026

Report MW5182113 · MDR key 24053725

Device

Generic name

Catheter, Peritoneal

Manufacturer

Conmed Corporation

Patient

30 YR · Female

  • Insufficient Information

Narrative

Description of Event or Problem

A REPOSABLE SUCTION CANNULA FROM A DIFFERENT MANUFACTURER DID NOT FIT PROPERLY (SCREW ON TO SUCTION IRRIGATOR TIP) AND AIR LEAKED CAUSING THE NORMAL SALINE TO HAVE A WEAK SPRAY AND IT SPITS. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).