MalfunctionFII
AQUARIUS - AUTOMATED FLUID
Received Jan 22, 2009 · Event occurred Nov 26, 2008
Report 6000002-2009-09719 · MDR key 1352944
Device
Generic name
Hemofiltration Machine
Manufacturer
Edwards LifesciencesModel number
GEF08200Catalog number
NA
Lot number
NA
Product problems
- Other (for use when an appropriate device code cannot be identified)
Patient
UNK
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
IT WAS REPORTED THAT TOO MUCH FLUID WAS BEING TAKEN FROM THE PATIENT. FILTRATION SCALE ON UPPER POINT OF CALIBRATION. NO PATIENT COMPLICATIONS WERE REPORTED.