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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:180062

Medtronic Open Pivot Aortic Valve Graft, REF 502AG25, SIZE 25 mm

Official recall number

Z-1533-2020

Evidence summary

Product code
LWQ
Recall status
Terminated
Event initiated
February 11, 2020
Root cause
Labeling mix-ups
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1533-2020

Field note

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