FDA Adverse Event Injury Summary report: N

EXTENSION SET

MDR report key: 2173915 · Received July 24, 2011

Report

Report Number
1423500-2011-09365
Event Type
Injury
Date Received
July 24, 2011
Date of Event
June 1, 2011
Report Date
June 28, 2011
Manufacturer
BAXTER HEALTHCARE - MOUNTAIN HOME
Product Code
KDJ
PMA / PMN Number
K925403
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A BATCH REVIEW WAS CONDUCTED FOR POTENTIALLY ASSOCIATED LOT NUMBERS H11E05047, H11D11089 AND H11C30081 WITH NO EXCEPTIONS OBSERVED RELATED TO THE REPORTED CONDITION. THE CAUSE OF THE PERITONITIS WAS UNDETERMINED. BAXTER HAS RECEIVED SIMILAR REPORTS FOR THE REPORTED PROBLEM. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS.

Additional Manufacturer Narrative · 1

(B)(4). AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN AND PATIENTS DISCARD SUPPLIES AFTER EACH THERAPY, THE SAMPLE WAS NOT REQUEST. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. THIS IS REPORT 3 OF 4 INVOLVED IN THIS PERITONITIS EVENT.

Description of Event or Problem · 1

THIS REPORT WAS RECEIVED FROM GLOBAL PHARMACOVIGILANCE (GPV) AND IS A SPONTANEOUS CONSUMER REPORT WITH SUPPLEMENTAL INFORMATION BY A NURSE FROM THE USA OF LOWER ABDOMINAL PAIN AND PERITONITIS WITH CULTURE POSITIVE FOR STAPHYLOCOCCUS EPIDERMIDIS IN A PATIENT COINCIDENT WITH DIANEAL PD2 AMBUFLEX THERAPY FOR PERITONEAL DIALYSIS (PD). DURING A CALL TO BAXTER CUSTOMER SERVICE, THE FOLLOWING WAS REPORTED. ON AN UNKNOWN DATE, THE PATIENT EXPERIENCED LOWER ABDOMINAL PAIN. ON (B)(6) 2011, THE PATIENT WAS HOSPITALIZED AND WAS BEING RULED OUT FOR PERITONITIS. FURTHER INFORMATION WAS RECEIVED FROM THE PD CLINIC SECRETARY AND THE PD NURSE WHO REPORTED ON (B)(6) 2011, THE PATIENT EXPERIENCED LOWER ABDOMINAL PAIN AND WAS HOSPITALIZED ON THE SAME DAY. ON AN UNKNOWN DATE IN 2011, THE PATIENT WAS DIAGNOSED WITH PERITONITIS WITH CULTURE POSITIVE FOR STAPHYLOCOCCUS EPIDERMIDIS. ON AN UNREPORTED DATE, THE PATIENT BEGAN TREATMENT WITH UNSPECIFIED IP ANTIBIOTICS (STOP DATE, FREQUENCY, AND DOSE NOT REPORTED). ON AN UNKNOWN DATE IN (B)(6) 2011, THE PATIENT WAS DISCHARGED FROM THE HOSPITAL AND HAD RECOVERED. DIANEAL THERAPY WAS ONGOING. THE HEALTHCARE PROFESSIONAL REPORTED THAT THE LOWER ABDOMINAL PAIN WAS UNRELATED TO DIANEAL THERAPY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 18 YR Hospitalization| R DIANEAL PD2 AMBUFLEX| HOMECHOICE