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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:147534

T090-000 90" 20 Drop IV Admin Set. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

Official recall number

Z-2223-2016

Evidence summary

Product code
FPA
Recall status
Terminated
Event initiated
June 14, 2016
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2223-2016

Field note

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