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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:155740

QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels

Official recall number

Z-2301-2017

Evidence summary

Product code
FOZ
Recall status
Terminated
Event initiated
March 20, 2017
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2301-2017

Field note

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