Siemens recalls MAMMOMAT Revelation breast imaging systems sold with bus-installation kits. These tables are designed for stationary use only and pose a risk if installed for bus applications.
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 MAM: MAMMOMAT Revelation breast imaging systems that were sold with bus-installation kits. These operator tables are designed for stationary use only and could malfunction if installed for bus applications.
The operator table was designed for stationary use only, not for bus installations. When sold with a bus-installation kit, it could become unstable or malfunction during mobile use, potentially causing injury.
Medical facilities that purchased MAMMOMAT Revelation systems with bus-installation kits are affected. Staff using these systems for mobile applications face the highest risk.
Check if your MAMMOMAT Revelation system (model 11343300) was sold with a bus-installation kit. Look for system serial numbers 1296, 10550, 10572, 10606, 10608, 11511, or 20140.
Verify if your MAMMOMAT Revelation system was sold with a bus-installation kit by checking the system serial numbers listed in the recall notice.
The operator table was designed for stationary use only and was sold with bus-installation kits, which could cause instability or malfunction during mobile applications.
Check if your MAMMOMAT Revelation system was sold with a bus-installation kit using the system serial numbers provided in the recall notice.
The recall notice does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Siemens Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0877-2026 — Siemens Medical Siemens Medical Hello, I own a Siemens Medical that is covered by recall Z-0877-2026 from Siemens Medical. 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.
