FDA Adverse Event Injury Summary report: N

MINICAP

MDR report key: 3020103 · Received March 25, 2013

Report

Report Number
1416980-2013-07170
Event Type
Injury
Date Received
March 25, 2013
Date of Event
February 21, 2013
Report Date
March 1, 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
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS REPORT OF PERITONITIS WAS RECEIVED WITH NO ALLEGED DEVICE MALFUNCTION OR USE ERROR; THEREFORE, A SAMPLE WAS NOT REQUESTED. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTIONS ARE REQUIRED. A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR ASSOCIATED LOT NUMBERS GD893446 AND GD893297 WITH NO ISSUES NOTED DURING THE MANUFACTURING PROCESS. THERE WERE NO DEVIATIONS FROM STANDARD PROCEDURE AND NO EXCEPTIONS RELATED TO THE REPORTED CONDITION WERE NOTED. SHOULD RELEVANT ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED AND WAS HOSPITALIZED FOR PERITONITIS COINCIDENT WITH THERAPY FOR CONTINUOUS CYCLER PERITONEAL DIALYSIS (CCPD). THE TREATMENT RENDERED WAS NOT REPORTED. THE CAUSE OF THE PERITONITIS WAS UNKNOWN. CCPD THERAPY WAS DISCONTINUED AS THE PATIENT HAD THEIR PD CATHETER REMOVED AND BEGAN HEMODIALYSIS. THE PATIENT WAS DISCHARGED FROM THE HOSPITAL AND WAS RECOVERING FROM THE PERITONITIS. THIS IS REPORT 2 OF 4 FOR THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
122167 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 70 YR Hospitalization DIANEAL PD4 ULTRABAG| HOMECHOICE, DIANEAL PD4 AMBUFLEX