FDA Adverse Event Malfunction Summary report: N

VISTA BASIC SAFETY INFUSION SYSTEM

MDR report key: 2151429 · Received June 20, 2011

Report

Report Number
1641965-2010-00094
Event Type
Malfunction
Date Received
June 20, 2011
Report Date
December 10, 2009
Manufacturer
B. BRAUN MEDICAL, INC.
Product Code
FRN
PMA / PMN Number
K003029
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DEVICE EVAL RESULTS: THIS INCIDENT WAS IDENTIFIED DURING AN AUDIT OF THE SERVICE NOTIFICATION DATABASE, AND HAS BEEN ADDED TO THE COMPLAINT TRACKING SYSTEM. AS THIS INCIDENT WAS ORIGINALLY PROCESSED THROUGH THE SERVICE DEPT., THE OPERATIONS LOG IS NOT AVAILABLE FOR REVIEW. B BRAUN COMPLETED AN EVAL OF THIS PUMP PER THE PROCEDURE FOR PUMP RETURNS, AND THE REPORTED FAILURE COULD NOT BE REPRODUCED. THE PUMP WAS TESTED PER THE ROUTINE REPAIR TESTING REQUIREMENTS. AS PART OF THE ROUTINE TESTING REQUIREMENTS, THE PUMP WAS TESTED FOR RATE ACCURACY THREE TIMES. IN EACH TEST, A VOLUME OF 25 ML WAS DELIVERED AT A RATE OF 125 ML/HR, WITH THE TIME SPECIFICATIONS OF 11:09 MIN - 12:18 MIN. ALL THREE TESTS PASSED WITH RESULTS OF 11:59, 11:48 AND 11:31. ROUTINE PREVENTIVE MAINTENANCE WAS PERFORMED ON THE PUMP, AND THE PUMP MET ALL FINAL INSPECTION CRITERIA. THE FACILITY REPORTED NO PT INJURY RELATED TO THIS COMPLAINT. THE PUMP WAS RETURNED TO THE CUSTOMER IN JAN 2010. SERIAL NUMBER HISTORY HAS SHOWN THAT, AS OF MAY 2011, THIS PUMP HAS NOT BEEN INVOLVED IN ANY FURTHER COMPLAINTS.

Description of Event or Problem · 1

THE PUMP WAS INFUSING SLOWER THAN IT SHOULD. WAS SET TO INFUSE IN 3 HRS; HOWEVER, IT INFUSED IN 4 HRS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VISTA BASIC SAFETY INFUSION SYSTEM INFUSION PUMP FRN B. BRAUN MEDICAL, INC. NA NA

Patients

Seq Age Sex Outcome Treatment
1 UNK