FDA Adverse Event Injury Summary report: N

MINICAP

MDR report key: 3961481 · Received July 28, 2014

Report

Report Number
1416980-2014-24459
Event Type
Injury
Date Received
July 28, 2014
Report Date
July 3, 2014
Manufacturer
BAXTER HEALTHCARE - CLEVELAND
Product Code
KDI
PMA / PMN Number
K895631
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS REPORT INVOLVES THE SAME PATIENT AS IN (B)(4). ON AN UNREPORTED DATE IN 2014, THE PATIENT EXPERIENCED PERITONITIS. A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBER GD896936 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. THE DEVICE WAS NOT RETURNED; THEREFORE, A DEVICE ANALYSIS COULD NOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT (PT) EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE CAUSE OF THE PERITONITIS WAS UNKNOWN, BUT WAS REPORTED BY THE PT TO BE DUE TO EATING LETTUCE AND THE BACTERIA ¿GOT INTO THE PERITONEUM.¿ IT WAS NOT REPORTED IF THE PATIENT WAS HOSPITALIZED FOR THE PERITONITIS EVENT. TREATMENT FOR THE PERITONITIS EVENT WAS NOT REPORTED. IT WAS NOT REPORTED IF THE PATIENT WAS RECOVERING OR HAD RECOVERED FROM THE PERITONITIS EVENT. IT WAS REPORTED THAT DIANEAL THERAPY WAS ONGOING. ADDITIONAL INFORMATION WAS REQUESTED BUT IS NOT AVAILABLE. THIS IS REPORT 2 OF 3.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
437508 MINICAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 Other CASSETTE, HOMECHOICE, MINICAP TRANSFER SET| DIANEAL LOW CALCIUM