ARTIS icono floor recall
ARTIS icono floor. Model Number: 11327700.
Why was ARTIS icono floor recalled?
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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.
- Product
- ARTIS icono floor. Model Number: 11327700.
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 30 units
- Distribution
- US Nationwide distribution.
- Recall date
- July 8, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)