inforMED
InjuryGBW

CATHETER, PERITONEAL

Received Aug 12, 2023

Report MW5139130 · MDR key 17532222

Device

Generic name

Catheter, Peritoneal

Manufacturer

Unknown

Product problems

  • Material Split, Cut or Torn
  • Material Split, Cut or Torn

Patient

Unknown

  • Peritonitis
  • Peritonitis

Narrative

Description of Event or Problem

THIS REPORT WAS RECEIVED FROM GLOBAL PHARMACOVIGILANCE (GPV) AND IS A SPONTANEOUS REPORT BY A CONSUMER IN THE USA OF PERITONITIS IN A PATIENT COINCIDENT WITH DIANEAL THERAPY FOR PERITONEAL DIALYSIS (PD). ON (B)(6) 2013, THE PATIENT EXPERIENCED PERITONITIS AND WAS HOSPITALIZED ON THE SAME DAY. THE CAUSE OF PERITONITIS WAS CUTTING OPEN THE CATHETER IN THE SHOWER. TREATMENT WAS NOT REPORTED. THE PATIENT WAS RECOVERING FROM THIS PERITONITIS EVENT. PATIENT INJURY REPORTED: YES. MEDICAL INTERVENTION REQUIRED: YES (B)(4). THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2).