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Siemens Medical Solutions USA, Inc recalls interventional fluoroscopic x-ray system
Recalled July 9, 2025 · FDA recall Z-2022-2025 · Siemens Medical Solutions USA
Hazard
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose. · FDA Class II
Sold at
Worldwide.
Description
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly report an application of a high dose.
Product
interventional fluoroscopic x-ray system
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →