Siemens ARTIS icono floor Recall Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Siemens Medical Solutions USA, Inc. is recalling 30 units of the ARTIS icono floor device due to potential loss of movement capability.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 7, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Siemens Medical Solutions USA, Inc. initiated a voluntary recall of the ARTIS icono floor device after identifying a potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Which Products Are Affected
The recall affects the ARTIS icono floor, Model Number: 11327700, with UDI-DI: 4056869149325. A total of 30 units distributed nationwide in the United States are involved. Affected serial numbers include: 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. The FDA recall number is Z-2643-2026, classified as Class II.
What You Should Do
Customers with affected units should contact Siemens Medical Solutions USA, Inc. regarding the recall.
Why This Matters
This Class II recall involves a device distributed across the United States where the identified issue could affect device functionality.
Source
FDA recall Z-2643-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,108 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.