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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:136622

Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the quantitative determination of the creatinine concentration in serum, plasma, and urine.

Official recall number

Z-1922-2015

Evidence summary

Product code
JJE
Recall status
Terminated
Event initiated
May 07, 2015
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1922-2015

Field note

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