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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:206201

MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776

Official recall number

Z-1347-2024

Evidence summary

Product code
DRE
Recall status
Open, Classified
Event initiated
January 30, 2024
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1347-2024

Field note

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