FDA Adverse Event Injury Summary report: N

RENAL - DISPOSABLE

MDR report key: 1911160 · Received November 30, 2010

Report

Report Number
1423500-2010-06388
Event Type
Injury
Date Received
November 30, 2010
Date of Event
November 1, 2010
Report Date
November 10, 2010
Product Code
KDJ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE DEVICES INVOLVED IN THE INCIDENT WERE UNKNOWN. AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUESTED. A 510(K) NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, A BATCH REVIEW WILL NOT BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. BAXTER WILL CONTINUE TO MONITOR SIMILAR REPORTS TO DETERMINE IF FURTHER ACTION IS REQUIRED.

Description of Event or Problem · 1

THIS IS A SPONTANEOUS REPORT BY A BAXTER EMPLOYEE NURSE FROM (B)(6) OF PERITONITIS IN A PATIENT COINCIDENT WITH PERITONEAL DIALYSIS (PD) THERAPY. ON (B)(6) 2010, THE PATIENT WAS DIAGNOSED WITH PERITONITIS, NOT REQUIRING HOSPITALIZATION. ON (B)(6) 2010, THE PATIENT WAS GIVEN A LOADING DOSE OF VANCOMYCIN 1GM IP AND BEGAN TREATMENT WITH "CIPTAZ" 4.5GM IP ONCE DAILY. THE ROOT CAUSE OF THE PERITONITIS WAS UNKNOWN. AT THE TIME OF REPORTING, THE OUTCOME OF THE PERITONITIS WAS UNKNOWN AND THE PATIENT CONTINUED TO RECEIVE REMEDIAL THERAPY WITH CIPTAZ. DIANEAL AND EXTRANEAL THERAPIES CONTINUED. THE REPORTER DID NOT PROVIDE AN ASSESSMENT OF CAUSALITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RENAL - DISPOSABLE SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ

Patients

Seq Age Sex Outcome Treatment
1 65 YR Required Intervention DIANEAL PD2 ULTRABAG AND EXTRANEAL VIAFLEX