FDA Adverse Event Injury Summary report: N

MINI-CAP, DISCONNECT W/PVP-1SOLUTION

MDR report key: 1994217 · Received February 17, 2011

Report

Report Number
1423500-2011-02069
Event Type
Injury
Date Received
February 17, 2011
Date of Event
January 1, 2011
Report Date
January 18, 2011
Manufacturer
BAXTER HEALTHCARE - CLEVELAND
Product Code
KDI
PMA / PMN Number
K895631
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CAUSE OF THE PERITONTIS WAS RELATED TO POOR ASEPTIC TECHNIQUE. A LABELING REVIEW WAS PERFORMED AND FOUND TO BE ADEQUATE. A BATCH REVIEW WAS PERFORMED FOR THE POTENTIALLY ASSOCIATED LOT NUMBER (GD878223), WITH NO DEFECT NOTED. BAXTER HAS CONDUCTED A TREND REVIEW AND FOUND THAT SIMILAR REPORTS HAVE BEEN RECEIVED FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS.

Additional Manufacturer Narrative · 1

(B)(4). THIS IS REPORT 3 OF 5 INVOLVED IN THIS PERITONITIS EVENT. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF BAXTER'S INVESTIGATION.

Description of Event or Problem · 1

DURING A FOLLOW-UP CALL FOR AN UNRELATED ALARM, THE PERITONEAL DIALYSIS (PD) NURSE REPORTED THE PATIENT WAS DIAGNOSED WITH PERITONITIS ON (B)(6) 2011. THE PATIENT WAS NOT HOSPITALIZED AND WAS TREATED WITH ANTIBIOTICS. THERE WAS NO EXIT SITE OR TUNNEL INFECTION. AN EFFLUENT SAMPLE WAS TAKEN PRIOR TO THE START OF ANTIBIOTICS. THE PATIENT BEGAN PD THERAPY THREE YEARS AGO. THE PD SOLUTION WAS NOT CONSIDERED SUSPECT AND WAS NOT STOPPED DUE TO THE PERITONITIS. THE PATIENT'S TRANSFER SET WAS REPLACED. THE NURSE STATED THE PERITONITIS WAS DUE TO A BREAK IN ASEPTIC TECHNIQUE AND THE PATIENT HAS BEEN RETRAINED. THE PERITONITIS IS ONGOING AND IMPROVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MINI-CAP, DISCONNECT W/PVP-1SOLUTION DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 69 YR Required Intervention DIANEAL SOLUTION, HOMECHOICE DEVICE