FDA Adverse Event Injury Summary report: N

MINICAP TRANSFER SET

MDR report key: 3041451 · Received April 8, 2013

Report

Report Number
1416980-2013-08746
Event Type
Injury
Date Received
April 8, 2013
Date of Event
February 28, 2013
Report Date
March 14, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
PMA / PMN Number
K882498
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PATIENT

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. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. 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 BATCH REVIEW WAS CONDUCTED FOR THE POTENTIALLY ASSOCIATED LOT NUMBER H12G27079, H12G31063 AND H12K09112. NO EXCEPTIONS WERE OBSERVED THAT WERE RELATED TO THE REPORTED CONDITION. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

THIS IS A REPORT OF PERITONITIS, COINCIDENT WITH DIANEAL THERAPIES FOR PERITONEAL DIALYSIS (PD). THE PATIENT EXPERIENCED PERITONITIS ON AN UNKNOWN DATE AND WAS HOSPITALIZED FOR THE EVENT. HOWEVER, THE TREATMENT WAS NOT REPORTED. THREE DAYS LATER, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL. THE PATIENT RECOVERED FROM THIS PERITONITIS EVENT. THIS IS REPORT 4 OF 4, FOR THE TRANSFER SET, IN THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
143768 MINICAP TRANSFER SET SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 68 YR Hospitalization DIANEAL PD4 ULTRABAG,| HOMECHOICE, DIANEAL PD4 AMBUFLEX