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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:202284

Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartPath to Ingenia Elition X)

Official recall number

Z-2398-2023

Evidence summary

Product code
LNH
Recall status
Open, Classified
Event initiated
June 12, 2023
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2398-2023

Field note

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