FDA Adverse Event Injury Summary report: N

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

MDR report key: 2212731 · Received August 16, 2011

Report

Report Number
1423500-2011-10749
Event Type
Injury
Date Received
August 16, 2011
Date of Event
July 1, 2011
Report Date
July 27, 2011
Manufacturer
BAXTER HEALTCARE
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 510K NUMBER WILL NOT BE PROVIDED IN THE MDR AS THE PRODUCT CODE AND LOT NUMBER ARE UNKNOWN. SINCE THE LOT NUMBER IS UNKNOWN, NO BATCH REVIEW WILL BE PERFORMED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS. THE ROOT CAUSE OF THE REPORTED CONDITION OF PERITONITIS IS UNDETERMINED.

Description of Event or Problem · 1

THIS REPORT WAS RECEIVED FROM GLOBAL PHARMACOVIGILANCE (GPV) AND IS A SPONTANEOUS REPORT BY A BAXTER EMPLOYED NURSE FROM (B)(6) OF PERITONITIS IN A PATIENT COINCIDENT WITH DIANEAL PD2 ULTRABAG THERAPY FOR PERITONEAL DIALYSIS (PD). ON (B)(6) 2011, THE PATIENT WAS DIAGNOSED WITH PERITONITIS, NOT REQUIRING HOSPITALIZATION. ON AN UNREPORTED DATE IN (B)(6) 2011, THE PATIENT RECEIVED TREATMENT WITH A LOADING DOSE OF VANCOMYCIN 2 GM IP, FOR THE PERITONITIS. ON AN UNREPORTED DATE IN 2011, THE EVENT OF PERITONITIS WAS CONSIDERED RESOLVING AND THE CAUSE OF THE PERITONITIS WAS UNKNOWN. DIANEAL THERAPY CONTINUED WITH DOSE UNSPECIFIED. THE NURSE BELIEVED THAT THE EVENT OF PERITONITIS WAS NOT RELATED TO THE SUSPECT PRODUCT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 38 YR Required Intervention DIANEAL PD2 ULTRABAG