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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:155727

Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Central Venous Catheter The Arrow¿ GlideThru" Peel-Away Sheath/Dilator Introducer is used for the percutaneous introduction of diagnostic or therapuetic devices into the vasculature.

Official recall number

Z-2288-2017

Evidence summary

Product code
FOZ
Recall status
Terminated
Event initiated
March 20, 2017
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2288-2017

Field note

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