FDA Adverse Event Injury Summary report: N

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

MDR report key: 3250984 · Received July 29, 2013

Report

Report Number
1416980-2013-19954
Event Type
Injury
Date Received
July 29, 2013
Date of Event
January 22, 2013
Report Date
July 2, 2013
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
FKX
PMA / PMN Number
K923065
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBERS H12I15021 AND H12J20012 WAS PERFORMED 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.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PERITONEAL DIALYSIS (PD) PATIENT EXPERIENCED PERITONITIS WHILE IN THE HOSPITAL FOR SEVERE BACK PAIN. THE NURSE REPORTED THE CAUSE OF THE PERITONITIS WAS DIARRHEA WHICH HAD CROSSED OVER THE PERITONEAL MEMBRANE. TREATMENT FOR THE PERITONITIS INCLUDED ZYBOX, ORAL (DOSE AND FREQUENCY NOT REPORTED). ON AN UNREPORTED DATE, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL. AT THE TIME OF THE INITIAL REPORT, THE PATIENT WAS NOT RECOVERED FROM THE PERITONITIS EVENT. THIS IS REPORT 1 OF 3 INVOLVED IN THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352940 HOMECHOICE AUTOMATED PD SET WITH CASSETTE SYSTEM, PERITONEAL, AUTOMATIC DELIVERY FKX BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 49 YR Required Intervention DIANEAL PD4, 2.5% AMBUFLEX, LOW CALCIUM| MINICAP TRANSFER SET| MINICAP| DIANEAL PD4, 4.25% AMBUFLEX, LOW CALCIUM