FDA Adverse Event Injury Summary report: N

MINICAP

MDR report key: 3113443 · Received May 15, 2013

Report

Report Number
1416980-2013-12354
Event Type
Injury
Date Received
May 15, 2013
Date of Event
April 11, 2013
Report Date
April 22, 2013
Manufacturer
BAXTER HEALTHCARE - CLEVELAND
Product Code
KDI
PMA / PMN Number
K895631
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

(B)(4). A BATCH REVIEW WAS CONDUCTED FOR THE POTENTIALLY ASSOCIATED LOT NUMBER GD893743. NO EXCEPTIONS WERE OBSERVED THAT WERE RELATED TO THE REPORTED CONDITION. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

Description of Event or Problem · 1

THIS IS REPORT 2 OF 2. THIS IS A REPORT OF PERITONITIS AND SEVERAL DIVERTICULI POPPED IN A PATIENT COINCIDENT WITH DIANEAL AND EXTRANEAL THERAPIES FOR PERITONEAL DIALYSIS (PD). ON AN UNREPORTED DATE, DIANEAL AND EXTRANEAL THERAPIES WERE WITHDRAWN. THE PATIENT EXPERIENCED CLOUDY PD EFFLUENT AND PAIN AND WAS HOSPITALIZED. THE PATIENT WAS DIAGNOSED WITH PERITONITIS. DURING HOSPITALIZATION IT WAS DETERMINED THAT SEVERAL DIVERTICULI HAD POPPED (RELATED TO DIVERTICULOSIS NOT DIVERTICULITIS). THE PATIENT WAS TREATED WITH UNSPECIFIED ANTIBIOTICS. THE PATIENT'S CATHETER WAS REMOVED, PD THERAPY ENDED AND THE PATIENT WAS PLACED ON HEMODIALYSIS. THE PATIENT WAS DISCHARGED HOME. THE PATIENT WAS RECOVERING FROM THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
215385 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 70 YR Hospitalization| R DIANEAL PD4 AMBUFLEX,EXTRANEAL VIAFLEX| HOMECHOICE