inforMED
InjuryGBW

CATHETER, PERITONEAL

Received Aug 12, 2023

Report MW5141330 · MDR key 17534429

Device

Generic name

Catheter, Peritoneal

Manufacturer

Unknown

Product problems

  • Fluid/Blood Leak
  • Fluid/Blood Leak

Patient

Unknown

  • Peritonitis
  • Peritonitis

Narrative

Description of Event or Problem

IT WAS REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE NURSE STATED THAT THE LEAK WAS COMING FROM THE PD CATHETER AND THAT THE PERITONITIS IS NOT RELATED TO BAXTER DEVICE, DISPOSABLES, OR DRUGS. THE NURSE STATED THAT SHE DOES NOT HAVE THE INFORMATION ABOUT THE CATHETER, INCLUDING THE MANUFACTURER. NO FURTHER INFORMATION WAS PROVIDED. PATIENT INJURY REPORTED: YES CMPLNT- (B)(4). THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).