WhichRecall
Class IIReported 2025-12-10

MAMMOMAT Revelation;

Recalled by Siemens Medical Solutions USA, Inc

Reason for Recall

There were instances where the operator table was sold together with a bus-installation kit

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The operator table is not intended and not released for bus installations as it was designed for stationary operation only.

Recall Number
Z-0877-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-10-24
Reported
2025-12-10
Distribution
Worldwide - US Nationwide distribution in the states of AR, CA, NY and the countries of Australia, Canada, India.
Code Info
Model Number: 11343300; UDI-DI: 04056869124575; System Serial Numbers: 1296, 10550, 10572, 10606, 10608, 11511, 20140;
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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