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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:145038

Vortex MEDICAL AngioVac Circuit, REF/UPN VTX3100, STERILE, Rx Only, Single Use Only -- The AngioVac Circuit and AngioVac Circuit Pack are designed to be used with the AngioVac Cannula.

Official recall number

Z-1701-2016

Evidence summary

Product code
DWE
Recall status
Terminated
Event initiated
March 21, 2016
Root cause
Environmental control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1701-2016

Field note

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