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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:161503

Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destination¿ Guiding Sheath is designed to be used for the introduction of interventional and diagnostic devices into the human vasculature, including but not limited to the renal, carotid, and peripheral arteries.

Official recall number

Z-0725-2018

Evidence summary

Product code
DYB
Recall status
Terminated
Event initiated
September 12, 2017
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0725-2018

Field note

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