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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:165305

Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized.

Official recall number

Z-3028-2018

Evidence summary

Product code
DWF
Recall status
Terminated
Event initiated
March 07, 2018
Root cause
Labeling False and Misleading
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-3028-2018

Field note

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