⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a
very recent recall may be missing. Everything shown is accurate as of the last checked time on this page —
for anything time-critical, confirm with the official sources linked below.
FDAClass II · Medical device · Recalled July 8, 2026
ARTIS icono floor recall — Siemens Medical Solutions USA, Inc
Hazard: Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Class II: may cause temporary or medically reversible health consequences.
View the official FDA enforcement record (openFDA) ↗
- Official recall ID
- Z-2643-2026
- Brand
- Siemens Medical Solutions USA
- Classification
- Class II
- Units affected
- 30 units
- Recall status
- Ongoing
- Initiated
- Voluntary: Firm initiated
Description
ARTIS icono floor. Model Number: 11327700.
Affected products
Companies & origin
- Recalling firm location
- Malvern, PA, United States
- Firm address
- 40 Liberty Blvd, N/A, 19355-1418
Identifying details (verbatim from the notice)
- Product codes / lots
- Model Number: 11327700. UDI-DI: 4056869149325. Serial Numbers: 174132, 174128, 174085, 174152, 174056, 174055, 174083, 174121, 174122, 174087, 174044, 174061, 174099, 174058, 174063, 174150, 174126, 174125, 174096, 174145, 174101, 174065, 174076, 174078, 174091, 174149, 174059, 174073, 174081, 174067.
- Distribution
- US Nationwide distribution.
- Firm notified the public via
- Letter
- FDA event ID
- 99079
- Recall initiated
- May 20, 2026
- FDA classified
- July 1, 2026
- FDA report date
- July 8, 2026
Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim;
the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.
Report a data error on this page