FDA Adverse Event Injury Summary report: N

NI

MDR report key: 6142189 · Received December 2, 2016

Report

Report Number
1416980-2016-17985
Event Type
Injury
Date Received
December 2, 2016
Report Date
December 2, 2016
Manufacturer
BAXTER HEALTHCARE CORPORATION
Product Code
KDJ
PMA / PMN Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TW
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE MEDIAN AGE WAS 43.6 ± 13.0 YEARS. THE OCCURRENCE DATE IS BETWEEN 2009 AND 2011. THE REPORTER IS ALSO AFFILIATED WITH THE FOLLOWING INSTITUTION: (B)(6). ARTICLE CITATION: CHENG-CHIA, LEE., KUN-HUA, TU., HSIAO-HUI, CHEN., MING-YANG, CHANG., CHENG-CHIEH, HUNG (2016). RISK FACTORS FOR DRAINAGE-REQUIRING ASCITES AFTER REFRACTORY PERITONITIS IN PERITONEAL DIALYSIS PATIENTS. INT UROL NEPHROL (2016) 48:1721¿1730. DOI 10.1007/S11255-016-1376-Y. THE SAMPLE WAS NOT RETURNED AND THE LOT NUMBER OF THE DEVICE WAS UNKNOWN; THEREFORE, A SAMPLE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED REFRACTORY PERITONITIS RESULTING IN SYMPTOMATIC ASCITES. THE CAUSE OF THE PERITONITIS WAS NOT REPORTED. THE PATIENT WAS HOSPITALIZED FOR THE EVENT AND WAS TREATED WITH UNSPECIFIED ANTIBIOTICS. ON AN UNREPORTED DATE THE PATIENT¿S PD CATHETER WAS REMOVED AND THE PATIENT WAS SWITCHED TO HEMODIALYSIS. SUBSEQUENTLY THE PATIENT DEVELOPED ASCITES REQUIRING PERCUTANEOUS DRAINAGE AND PROLONGED HOSPITALIZATION. THE PATIENT OUTCOME WAS NOT REPORTED. ADDITIONAL INFORMATION IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
792479 NI SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE CORPORATION NA NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R EXTRANEAL