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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:187483

Medtronic HY8M63R4, Custom Pack HY8M63R4 Adult ECC, Custom Perfusion System, Sterile, Rx.

Official recall number

Z-1872-2021

Evidence summary

Product code
DWF
Recall status
Terminated
Event initiated
April 29, 2021
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1872-2021

Field note

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