FDA Adverse Event Injury Summary report: N

BICART

MDR report key: 3234055 · Received July 18, 2013

Report

Report Number
9616023-2013-00004
Event Type
Injury
Date Received
July 18, 2013
Date of Event
June 15, 2013
Report Date
June 18, 2013
Manufacturer
GAMBRO LUNDIA AB
Product Code
KPO
PMA / PMN Number
K013724
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE BICART PRODUCT INVOLVED IN THIS INCIDENT WAS NOT AVAILABLE FOR INVESTIGATION AND THE BICART MODEL AND LOT NUMBER COULD NOT BE PROVIDED BY THE FACILITY. GAMBRO HAS NO INFORMATION TO SUGGEST THAT THE BICART PRODUCT CAUSED OR CONTRIBUTED TO THE INCIDENT AND GAMBRO DOES NOT REGARD THE SUBMITTAL OF THIS REPORT AS AN ADMISSION OF CAUSATION OR LIABILITY.

Description of Event or Problem · 1

A PATIENT WAS ADMITTED TO THE ICU AFTER EVALUATION IN THE ER FOR LETHARGY, HYPERTENSION AND HYPERKALEMIA. THE PATIENT HAS A HISTORY OF CHRONIC RENAL FAILURE AND CHRONIC DIALYSIS BUT WAS UNKNOWN TO THE FACILITY AND NEPHROLOGY GROUP. UPON ADMISSION TO THE ICU, THE PHYSICIAN ORDERED A DIALYSIS TREATMENT FOR THE PATIENT. WITHIN THE FIRST FEW MINUTES OF THE DIALYSIS TREATMENT, THE PATIENT BECAME RESTLESS, SAT UP IN BED SCREAMING, HAD AN INCREASE IN BLOOD PRESSURE, EXPERIENCED A SEIZURE AND CODED. THESE SYMPTOMS ARE CONSISTENT WITH A TYPE A DIALYZER REACTION WHICH IS AN ALLERGIC REACTION TO THE DIALYZER. THERE HAD BEEN NO PROBLEMS OR MACHINE ALARMS DURING THE TREATMENT. THE BLOOD FROM THE EXTRACORPOREAL CIRCUIT WAS RETURNED TO THE PATIENT AND TREATMENT ENDED. THE PATIENT WAS SUCCESSFULLY RESUSCITATED. THE INVOLVED BLOOD TUBING SET, BICART AND DIALYZER WERE DISCARDED AND WILL NOT BE RETURNED TO GAMBRO.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
333439 BICART DIALYSATE CONCENTRATE FOR HEMODIALYSIS (LIQUID OR POWDER) KPO GAMBRO LUNDIA AB UNK

Patients

Seq Age Sex Outcome Treatment
1 25 YR Required Intervention