Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MAGNETOM Aera magnetic resonance system. Indicated for use as a Recalled by Siemens Medical Solutions USA, Inc Due to Siemens discovered a processing error for the MAGNETOM...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.
Affected Products
MAGNETOM Aera magnetic resonance system. Indicated for use as a magnetic resonance diagnostic device (MRDD) that produces transverse, sagittal, coronal and oblique cross sectional images, spectroscopic images and/or spectra, and that displays the internal structure and/or function of the head, body, or extremities.
Quantity: 5
Why Was This Recalled?
Siemens discovered a processing error for the MAGNETOM Aera magnetic resonance system that may have resulted in some users not receiving Operator Manuals.
Where Was This Sold?
This product was distributed to 5 states: CA, CO, IA, MN, TX
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report