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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209921

Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782105

Official recall number

Z-3196-2024

Evidence summary

Product code
LNH
Recall status
Open, Classified
Event initiated
September 03, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-3196-2024

Field note

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