VISTA BASIC SAFETY INFUSION SYSTEM
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
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.
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 |