Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643 Recalled by Siemens Medical Solutions USA, Inc Due to Potential of an open port in the quench...
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 Spectra magnetic resonance diagnostic devices Model # 10837643
Quantity: 2
Why Was This Recalled?
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Where Was This Sold?
This product was distributed to 41 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MO, MT, NE, NH, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, VA, WA, WV, WI, WY, DC
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