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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:156508

18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

Official recall number

Z-2716-2017

Evidence summary

Product code
FMG
Recall status
Terminated
Event initiated
May 30, 2017
Root cause
Nonconforming Material/Component
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2716-2017

Field note

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