InjuryFII
AQUARIUS (W/CITRATE OPTION)
Received Nov 26, 2008 · Event occurred Oct 28, 2008
Report 6000002-2008-09363 · MDR key 1246358
Device
Generic name
Hemofiltration Machine
Manufacturer
Edwards LifesciencesModel number
GEF09500Catalog number
NA
Lot number
NA
Product problems
- Occlusion, incorrect
Patient
UNK
- No Consequences Or Impact To Patient
Narrative
Description of Event or Problem
REPORTEDLY, THERE WAS A LONG THROMBUS IN VENOUS LINE DURING CITRATE ANTICOAGULATION.
Additional Manufacturer Narrative
DEVICE NOT RETURNED.