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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:170630

Urethral Dilation Balloon Catheter with Open Tip , Global Product No. G17844

Official recall number

Z-0970-2020

Evidence summary

Product code
KOE
Recall status
Terminated
Event initiated
January 04, 2019
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0970-2020

Field note

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