CATHETER, PERITONEAL
Received Aug 12, 2023
Report MW5139130 · MDR key 17532222
Device
Generic name
Catheter, Peritoneal
Manufacturer
UnknownProduct 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).