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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:166148

HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath Introducer System, Material HO-14702 The central venous catheter permits venous access to the central circulation through an indwelling Arrow percutaneous sheath introducer.

Official recall number

Z-2818-2018

Evidence summary

Product code
FOZ
Recall status
Terminated
Event initiated
July 10, 2018
Root cause
Under Investigation by firm
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2818-2018

Field note

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