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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:180797

HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch, Product Code: M00202175832P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.

Official recall number

Z-1874-2020

Evidence summary

Product code
MAL
Recall status
Terminated
Event initiated
April 07, 2020
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1874-2020

Field note

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