Siemens Medical Solutions USA, Inc recalls Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Mod…
- Recall date
- July 2, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2525-2024
- FDA classification
- Class II
- Brand / firm
- Siemens Medical Solutions USA, Inc
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image. Model Number: 10762472
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