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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:165530

30 cm (12") PUR Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, 2 NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system.

Official recall number

Z-2799-2018

Evidence summary

Product code
FMG
Recall status
Terminated
Event initiated
March 01, 2018
Root cause
Other
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2799-2018

Field note

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