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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:149658

Custom Arterial Pack, kit number RMS1712(F convenience custom kits used for general surgery in hospital operating room

Official recall number

Z-0163-2017

Evidence summary

Product code
FSY
Recall status
Terminated
Event initiated
April 22, 2015
Root cause
Unknown/Undetermined by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0163-2017

Field note

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