FDA recall Z-2022-2025

Siemens Medical Solutions USA, Inc · Class II · device

Product

interventional fluoroscopic x-ray system

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.

Key facts

Status
Ongoing
Initiation date
2025-05-15
Report date
2025-07-09
Voluntary/Mandated
FDA Mandated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2022-2025