Class II

Medical Device Recall: interventional fluoroscopic x-ray system

Siemens Medical Solutions USA, Inc · May 15, 2025

Reason for Recall

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.

Distribution

Worldwide.

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2022-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.