FDA Adverse Event Injury Summary report: N

MINICAP TRANSFER SET

MDR report key: 4140822 · Received October 3, 2014

Report

Report Number
1416980-2014-34421
Event Type
Injury
Date Received
October 3, 2014
Date of Event
September 9, 2014
Report Date
September 10, 2014
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AG
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE REPORTED PRODUCT IS AN UNKNOWN BAXTER TRANSFER SET. AS THE SAMPLE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN, A DEVICE EVALUATION CANNOT BE COMPLETED. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS THERAPY. THE PERITONITIS WAS MANIFESTED BY CLOUDY EFFLUENT. THE CAUSE OF THE PERITONITIS WAS UNKNOWN AND THE PATIENT WAS NOT HOSPITALIZED FOR THE EVENT. THE PATIENT WAS TREATED WITH CEFACIDALE AND GENTAMYCIN (DOSE, ROUTES, FREQUENCIES, AND DURATIONS NOT REPORTED) FOR THE PERITONITIS. THE PATIENT WAS REPORTED TO HAVE RECOVERED FROM THE PERITONITIS. ACTION TAKEN WITH PERITONEAL DIALYSIS THERAPY WAS NOT REPORTED. ADDITIONAL INFORMATION WAS NOT AVAILABLE. THIS IS REPORT 1 OF 3 INVOLVED IN THIS PERITONITIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
619614 MINICAP TRANSFER SET SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - MOUNTAIN HOME

Patients

Seq Age Sex Outcome Treatment
1 48 YR Required Intervention MINICAP, TITANIUM ADAPTER| COVIDIEN PLASTIC ADAPTER| 55 C DIALYSE SOL