FDA Adverse Event Injury Summary report: N

NXSTAGE SYSTEM ONE

MDR report key: 1140951 · Received August 28, 2008

Report

Report Number
3003464075-2008-00403
Event Type
Injury
Date Received
August 28, 2008
Date of Event
August 3, 2008
Report Date
August 3, 2008
Manufacturer
NXSTAGE MEDICAL, INC.
Product Code
KDI
PMA / PMN Number
K050525
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

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 PT'S BLOOD IN THE EVENT OF AN UNRECOVERABLE ALARM. THE AIR ALARM IS MOST LIKELY DUE TO AIR ENTERING THE CIRCUIT DURING TROUBLESHOOTING AND RECONNECTING FOR TREATMENT. THE DISPOSABLE CARTRIDGE WAS NOT AVAILABLE FOR EVAL. OCCASIONAL ALARMS DURING HEMODIALYSIS TREATMENTS ARE EXPECTED, AND SHOULD NOT RESULT IN BLOOD LOSS IF DEVICE LABELING INSTRUCTIONS ARE FOLLOWED. A DIRECT CORRELATION BETWEEN NXSTAGE SYSTEM ONE AND THE REPORTED BLOOD LOSS CANNOT BE ESTABLISHED. FACILITY STAFF HAS BEEN NOTIFIED OF THE EVENT. NXSTAGE MEDICAL CONSIDERS THIS REPORT CLOSED. NO ADD'L INFO WILL BE PROVIDED.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AS AN ADVERSE EVENT SOLELY TO COMPLY WITH THE FDA'S BLOOD LOSS POLICY. THE OPERATOR HAD BEEN IN RECIRCULATION MODE DURING A ROUTINE HEMODIALYSIS TREATMENT. WHEN RECONNECTING, MULTIPLE VENOUS AIR ALARMS OCCURRED FOLLOWED BY LOW VENOUS PRESSURE ALARMS. RINSEBACK WAS NOT PERFORMED DUE TO POSSIBLE CLOTTING OF THE CIRCUIT, 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 UNK

Patients

Seq Age Sex Outcome Treatment
1 44 YR Other