Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:120889

ACL TOP 700; PN 0000280010 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or fibrinolysis testing in the assessment of thrombosis and/or hemostasis. The systems provide results for both direct hemostasis measurements and calculated parameters.

Official recall number

Z-2245-2013

Evidence summary

Product code
GKP
Recall status
Terminated
Event initiated
July 19, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2245-2013

Field note

Send feedback

We'll only use this to respond to your feedback.