Use cautionMedical device recall · FDA · Published October 24, 2025
Siemens MAMMOMAT Inspiration: Operator Table Not for Bus Installations
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.
Take action
Contact the company
📍Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd · Malvern, PA 19355-1418
“Siemens MAMMOMAT Inspiration: Operator Table Not for Bus Installations.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/51005-siemens-mammomat-inspiration-operator-table-not-for-bus-installations. Based on FDA recall #Z-0878-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0878-2026%22&limit=1).
The FDA announced on Oct. 24, 2025, that Siemens Medical Solutions USA, Inc. is recalling MAMMOMAT Inspiration systems because the operator table was incorrectly sold with a bus-installation kit intended for stationary use only. This Class II recall affects six units distributed in Arkansas, California, New York, Australia, Canada, and India.
How to tell if you have it
Brand: Siemens
Product: MAMMOMAT Inspiration
Model Number: 10140000
UDI-DI: 04056869009063
System Serial Numbers: 6734, 6694, 10121, 10309, 10336, 10342
The hazard
The hazard involves the operator table being sold together with a bus-installation kit. The device is designed for stationary operation only and was not released for bus installations.
Context
GovInfoNow's records show Siemens Medical Solutions USA, Inc. has 182 other recalls on record since June 6, 2017. Other recent recalls of similar products include the Siemens ARTIS icono Ceiling Monitor Recall regarding loose screws (June 8, 2026), the Siemens ARTIS icono ceiling recall for loss of movement after extreme height adjustments (May 20, 2026), and the Siemens ARTIS Pheno VE30A/VE40A recall for inaccurate 3D scans due to radiation exposure (March 12, 2026).
How to tell if you have this one
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.
Brand
Siemens
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution in the states of AR, CA, NY and the countries of Australia, Canada, India.
Recall number
Product, codes & lots
Quantity
Z-0877-2026
MAMMOMAT Revelation;; Model Number: 11343300; UDI-DI: 04056869124575; System Serial Numbers: 1296, 10550, 10572, 10606, 10608, 11511, 20140;
7 units (3 US, 4 OUS)
Z-0878-2026
MAMMOMAT Inspiration;; Model Number: 10140000; UDI-DI: 04056869009063; System Serial Numbers: 6734, 6694, 10121, 10309, 10336, 10342;
6 units (3 US, 3 OUS)
Z-0879-2026
MAMMOMAT Fusion;; Model Number: 10140000; UDI-DI: 04056869009063; System Serial Numbers: 10559;
1 unit (OUS only)
Based on the official FDA remedy
What to do — step by step
Check for Bus-Installation Kit
If your MAMMOMAT Inspiration has a bus-installation kit, it is part of the recall and should not be used for bus installations.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of AR, CA, NY and the countries of Australia, Canada, India.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arkansas, California, New York.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-0878-2026 (October 24, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0878-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.