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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:162509

IMMULITE ¿ /IMMULITE ¿ 1000 CEA

Official recall number

Z-1678-2018

Evidence summary

Product code
DHX
Recall status
Terminated
Event initiated
January 02, 2018
Root cause
Error in labeling
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-1678-2018

Field note

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