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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:169037

ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of homocysteine in human serum, heparinized plasma or EDT A plasma on TOSOH AIA System Analyzers. Homocysteine measurements are used in the diagnosis and treatment of hyperhomocysteinemia or homocysteinuria.

Official recall number

Z-0675-2019

Evidence summary

Product code
LPS
Recall status
Terminated
Event initiated
November 30, 2018
Root cause
Device Design
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0675-2019

Field note

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