RecallRadar

FDA Device recall Z-2528-2024

Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700

On 2024-08-14 the FDA classified a Class II recall of Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700 by Siemens Medical Solutions Usa, citing the support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2528-2024
ClassificationClass II
Statusongoing
Initiated2024-07-02
Published2024-08-14
Last updated2026-09-13 11:57 UTC
CompanySiemens Medical Solutions Usa
DistributionUS

Product

Multitom Rax -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image Model Number: 10860700

Reason

The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays

Identifiers

code_info
UDI: N/A Serial Numbers: * Multitom Rax systems are licensed for sale in the US but have not been identified as being a…UDI: N/A Serial Numbers: * Multitom Rax systems are licensed for sale in the US but have not been identified as being affected by this recall issue in the United States. However, this system is included in the event affected systems are identified in the future.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2528-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.