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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:206797

Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003

Official recall number

Z-1799-2024

Evidence summary

Product code
DWF
Recall status
Open, Classified
Event initiated
March 19, 2024
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1799-2024

Field note

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