INFUSION PUMP
Report
- Report Number
- 6000001-2009-00276
- Event Type
- Malfunction
- Date Received
- March 31, 2009
- Date of Event
- March 13, 2009
- Report Date
- March 13, 2009
- Manufacturer
- BAXTER HEALTHCARE - SINGAPORE
- Product Code
- FRN
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
BAXTER HAS NOT RECEIVED THE DEVICE FOR EVAL. THE CUSTOMER STATED THE DEVICE WILL NOT BE RETURNED TO BAXTER FOR EVAL. A FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFO BECOMES AVAILABLE.
THE CUSTOMER REPORTED THE NURSE SPIKED THE MINI-BAG AND PROGRAMMED THE FLO-GARD INFUSION PUMP. SERIAL NUMBER UNK, TO HAVE THE BAG RUN DRY. THEY DO THIS BY PROGRAMMING THE VTBI (VOLUME TO BE INFUSED) TO BE GREATER THAN THE AMOUNT OF SOLUTION BAG. WHEN THE PUMP COMPLETED THE INFUSION AND RAN THE BAG DRY, THE NURSE EITHER DISCOVERED OR WAS ALERTED BY THE PT'S FAMILY MEMBER TO THE EMPTY THE BAG. THE BAG AND UPSTREAM TUBING WERE FOUND EMPTY. FLUID IS STILL PRESENT IN THE DOWNSTREAM TUBING AND APPEARS TO BE "PULSATING". BLOOD WAS ALSO PULSATING AT THE PT IV SITE. THE PUMP DID NOT ALARM AT THIS POINT. THE NURSE REMOVED THE TUBING FROM THE PUMP AND DISCOVERED THE TUBING IS EMPTY AND FLAT. THERE WAS NO PT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS REPORT. THIS CONDITION OCCURRED WHILE ADMINISTERING DEXAMETHASONE TO A PT FROM THE 50ML MINI-BAG VIAFLEX, PRODUCT CODE 2B1308, LOT NUMBER P232405, IN 2009. THE CUSTOMER BELIEVES THIS ISSUE IS RELATED TO USE OF THIS 50ML MINI-BAG SINCE THEY BEGAN EXPERIENCING THIS ISSUE UPON INTRODUCING THIS PRODUCT INTO THEIR PROCESS. THIS CONDITION ONLY OCCURS WITH MINI-BAGS THAT ARE NOT PRE-PRIMED BY THE PHARMACY. NO ADDITIONAL INFO IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INFUSION PUMP | 80FRN | FRN | BAXTER HEALTHCARE - SINGAPORE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |