Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0878-2026 — MAMMOMAT Inspiration;

U.S. FDA — Device Enforcement · United States · 2025-10-24 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0878-2026
Date of alert: 2025-10-24
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Siemens Medical Solutions USA, Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10140000

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0878-2026 — MAMMOMAT Inspiration;

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