Siemens Medical Solutions USA, Inc SOMATOM Force; the intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angels or spiral planes taken at different angles. Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SOMATOM Force; the intended use of computed tomography is to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angels or spiral planes taken at different angles.
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Model number: 10742326, serial numbers 75437, 75454, 75464, 75450, 75467, 75475, 75439.
Products Sold
Model number: 10742326, serial numbers 75437, 75454, 75464, 75450, 75467, 75475, 75439.
Siemens Medical Solutions USA, Inc is recalling SOMATOM Force; the intended use of computed tomography is to produce cross-sectional images of the b due to Artifacts are found in acquired imaging on the SOMATOM Force.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Artifacts are found in acquired imaging on the SOMATOM Force.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
MD, MA, MN, PA, SC, TX
Page updated: Jan 12, 2026