Siemens recalls MAMMOMAT Inspiration models sold with bus-installation kits. These operator tables are designed for stationary use only and not safe for bus installations.
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.
Siemens is recalling MAMMOMAT Inspiration breast cancer screening machines that were sold with bus-installation kits. These operator tables are designed for stationary use only and could be unsafe if installed on a bus.
The operator table was designed for stationary use only and not intended for bus installations. When sold with a bus-installation kit, it may not function safely in mobile environments.
Owners of MAMMOMAT Inspiration models sold with bus-installation kits are affected. Medical facilities using these machines for mobile applications are at higher risk.
Check for MAMMOMAT Inspiration models with serial numbers 6734, 6694, 10121, 10309, 10336, or 10342. These units were sold with bus-installation kits and are not safe for bus use.
If your MAMMOMAT Inspiration has a bus-installation kit, it is part of the recall and should not be used for bus installations.
The operator table was designed for stationary use only and not intended for bus installations, so it could be unsafe when used with a bus-installation kit.
MAMMOMAT Inspiration models with serial numbers 6734, 6694, 10121, 10309, 10336, or 10342.
No, if the machine was sold with a bus-installation kit, it should not be used for bus installations as it is designed for stationary use only.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0878-2026 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0878-2026 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
