FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 4112274 · Received September 23, 2014

Report

Report Number
1416980-2014-32944
Event Type
Injury
Date Received
September 23, 2014
Date of Event
August 21, 2014
Report Date
August 29, 2014
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
PMA / PMN Number
K894783
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE REPORTED PRODUCT IS AN UNKNOWN BAXTER TITANIUM ADAPTER. THE DEVICE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN, THEREFORE, A DEVICE ANALYSIS CANNOT BE COMPLETED. THE CAUSE IS NOT IDENTIFIED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A FOLLOW-UP WILL BE SUBMITTED. SAME PATIENT AS (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF THE PERITONITIS WAS UNKNOWN. THE PATIENT WAS HOSPITALIZED FOR THE EVENT. ON AN UNREPORTED DATE, THE PATIENT WAS TREATED FOR THE PERITONITIS WITH UNKNOWN ANTIBIOTICS (DOSE, ROUTE AND FREQUENCY NOT REPORTED). ONE DAY AFTER BEING ADMITTED, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL. ON AN UNREPORTED DATE, DIANEAL THERAPIES WERE DISCONTINUED AND THE PATIENT WAS PUT ON HEMODIALYSIS FOR A FEW WEEKS WHILE RECOVERING FROM THE EVENT. AT THE TIME OF THIS REPORT, THE PATIENT WAS RECOVERED FROM THE PERITONITIS. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. THIS IS REPORT 2 OF 4 INVOLVED IN THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
592542 SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 53 YR Hospitalization| R DIANEAL 1.5% & 2.5% PD4 AMBUFLEX| TRANSFER SET, CASSETTE, MINICAP, HOMECHOICE