MalfunctionGBW
CORE REPOSAL TRUMPET
Received Jan 13, 2026
Report MW5182113 · MDR key 24053725
Device
Generic name
Catheter, Peritoneal
Manufacturer
Conmed CorporationModel number
CONMED CORE REPOSAL TRUMPETPatient
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).