FDA Adverse Event Injury Summary report: N

MINI-CAP

MDR report key: 3051428 · Received April 10, 2013

Report

Report Number
1416980-2013-08988
Event Type
Injury
Date Received
April 10, 2013
Date of Event
March 8, 2013
Report Date
March 21, 2013
Manufacturer
BAXTER HEALTHCARE - CLEVELAND
Product Code
KDI
PMA / PMN Number
K895631
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

(B)(4). AS THE SAMPLE WAS NOT RETURNED AND THE LOT NUMBER IS UNKNOWN, A DEVICE ANALYSIS CANNOT BE COMPLETED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. SAME PATIENT AS (B)(4).

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

(B)(4). THE FOLLOWING INFORMATION IS FROM THE NURSE. THE PATIENT WAS TREATED WITH VANCOMYCIN BY INTRAPERITONEAL INJECTION, 1.5 GRAM(GM) FOR 4 WEEKS. THE PATIENT DENIED TOUCH CONTAMINATION. THE PATIENT WAS RETRAINED AND RECOVERED FROM THE EVENT OF PERITONITIS. A REVIEW OF ALL BATCH RECORD DOCUMENTS WAS PERFORMED FOR POTENTIALLY ASSOCIATED LOT NUMBERS GD893743 AND GD893735 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 THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE PATIENT WAS HOSPITALIZED FOR THE EVENT. THE CAUSE OF PERITONITIS WAS NOT REPORTED. TREATMENT WAS NOT REPORTED. THE PATIENT WAS RECOVERING. THIS IS REPORT 2 OF 4.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
153501 MINI-CAP DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM KDI BAXTER HEALTHCARE - CLEVELAND

Patients

Seq Age Sex Outcome Treatment
1 56 YR Hospitalization DIANEAL PD2 AMBUFLEX AND DIANEAL PD2 ULTRABAG