FDAMay 15, 2025device

interventional fluoroscopic x-ray system

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

siemens medical solutionssiemenssiemens medical

UPCs

4056869295923

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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