BICART
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
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.
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 |