NXSTAGE SYSTEM ONE
Report
- Report Number
- 3003464075-2008-00466
- Event Type
- Injury
- Date Received
- October 7, 2008
- Date of Event
- September 9, 2008
- Report Date
- September 9, 2008
- Manufacturer
- NXSTAGE MEDICAL, INC.
- Product Code
- KDI
- PMA / PMN Number
- K050525
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- NOT APPLICABLE
Narratives
THERE IS NO EVIDENCE OF A DEVICE MALFUNCTION. THE REPORTED BLOOD LOSS IS ATTRIBUTED TO THE OPERATOR NOT PERFORMING RINSEBACK IN A TIMELY MANNER. THE USER'S GUIDE INSTRUCTS THE OPERATOR TO PROMPTLY RINSEBACK THE PATIENT'S BLOOD IN THE EVENT OF AN UNRECOVERABLE ALARM. THE ALARM IS ATTRIBUTED TO USER ERROR AS THE OPERATOR INADVERTENTLY CLAMPED THE ARTERIAL LINE WHILE THE PUMP WAS RUNNING. THE CYCLER ALARMED APPROPRIATELY. A DIRECT CORRELATION BETWEEN NXSTAGE SYSTEM ONE AND THE REPORTED BLOOD LOSS CANNOT BE ESTABLISHED. FACILITY STAFF HAS BEEN NOTIFIED AND REVIEWED THE EVENT WITH THE OPERATOR. NXSTAGE MEDICAL CONSIDERS THIS REPORT CLOSED. NO ADDITIONAL INFORMATION WILL BE PROVIDED.
THIS REPORT IS BEING FILED AS AN ADVERSE EVENT SOLELY TO COMPLY WITH THE FDA'S BLOOD LOSS POLICY. DURING A ROUTINE HEMODIALYSIS TREATMENT, THE OPERATOR INADVERTENTLY CLAMPED THE ARTERIAL LINE WHILE THE PUMP WAS STILL RUNNING, CAUSING AN ARTERIAL PRESSURE ALARM. CLOTTING OF THE CIRCUIT OCCURRED DUE TO THE AMOUNT OF TIME SPENT TROUBLESHOOTING THE ALARM. RINSEBACK WAS NOT PERFORMED RESULTING IN AN ESTIMATED BLOOD LOSS OF 190CC. NO MEDICAL INTERVENTION WAS REQUIRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NXSTAGE SYSTEM ONE | HIGH PERMEABILITY HEMODIALYSIS SYSTEM | KDI | NXSTAGE MEDICAL, INC. | CAR-170 | 7087708 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 38 YR | Other |