FDA Adverse Event Injury Summary report: N

FLEXICAP

MDR report key: 3092200 · Received May 3, 2013

Report

Report Number
1416980-2013-11235
Event Type
Injury
Date Received
May 3, 2013
Date of Event
March 19, 2013
Report Date
April 10, 2013
Manufacturer
BAXTER HEALTHCARE - SWINFORD
Product Code
KDJ
PMA / PMN Number
K972579
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A REVIEW OF ALL BATCH RECORD DOCUMENTS FOR POTENTIALLY ASSOCIATED LOT NUMBER, 12I18H25 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. SHOULD ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. THIS IS THE SAME PATIENT AS (B)(4).

Additional Manufacturer Narrative · 1

(B)(4): THE CAUSE OF PERITONITIS WAS UNKNOWN. ON AN UNREPORTED DATE, THE PATIENT WAS RETRAINED ON A PROPER ASEPTIC TECHNIQUE. THE PATIENT RECOVERED FROM PERITONITIS.

Description of Event or Problem · 1

THE CULTURE WAS PERFORMED ON (B)(6) 2013.

Description of Event or Problem · 1

THIS IS REPORT 3 OF 4. IT WAS REPORTED THAT THE PATIENT EXPERIENCED PERITONITIS COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. THE PATIENT HAD SYMPTOMS OF ABDOMINAL PAIN AND CLOUDY EFFLUENT. THE PATIENT WAS TREATED WITH ANCEF 1500 MILLIGRAMS INTRAPERITONEAL (IP) DAILY FOR 3 DAYS AND GENTAMYCIN 40 MILLIGRAM IP DAILY. AFTER CULTURES RESULTS WERE NEGATIVE, ANCEF WAS STARTED AS 1 GRAM DAILY IP FOR 5 DAYS. THE PATIENT IS CONSIDERED TO BE RECOVERED FROM THIS EVENT AND THE CAUSE OF PERITONITIS IS UNKNOWN. PD THERAPY WAS ONGOING DURING THE EVENT OF PERITONITIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
193984 FLEXICAP SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - SWINFORD

Patients

Seq Age Sex Outcome Treatment
1 59 YR Required Intervention AMBUFLEX, EXTRANEAL