FDA Adverse Event Injury Summary report: N

CAPD DISCONNECT Y SET

MDR report key: 3023334 · Received March 27, 2013

Report

Report Number
1416980-2013-07412
Event Type
Injury
Date Received
March 27, 2013
Report Date
March 7, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
PMA / PMN Number
K961825
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBER(S) H12K07124 AND H12L15075 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.

Additional Manufacturer Narrative · 1

(B)(4): THE OCCURRENCE DATE FOR THE PERITONITIS EVENT IS UNKNOWN. (B)(4). THIS REPORT OF PERITONITIS WAS RECEIVED WITH NO ALLEGED DEVICE MALFUNCTION OR USE ERROR; THEREFORE, A SAMPLE WAS NOT REQUESTED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

THIS IS REPORT 4 OF 4 FOR THIS PERITONITIS EVENT. THIS IS A REPORT OF PERITONITIS IN A PATIENT COINCIDENT WITH PERITONEAL DIALYSIS (PD). ON AN UNKNOWN DATE DURING HOSPITALIZATION FOR AN UNRELATED ISSUE, THE PATIENT WAS DIAGNOSED WITH PERITONITIS. THE TREATMENT FOR THE PERITONITIS INCLUDED UNSPECIFIED IV ANTIBIOTICS. THE PATIENT'S PD CATHETER WAS REMOVED, PD THERAPY WAS DISCONTINUED, AND HEMODIALYSIS WAS STARTED. THE PATIENT WAS RECOVERING FROM THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
127229 CAPD DISCONNECT Y SET SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention DIANEAL PD4 AMBUFLEX