FDA Device recall Z-1795-2013
Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003
- FDA Device
- Class II
- terminated
- Published 2013-07-31
On 2013-07-31 the FDA classified a Class II recall of Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003 by Siemens Medical Solutions Usa, citing siemens issued a Field Safety Notice about the potential hazard to patients or operators when using the function "table top float" of the AXIOM Aristos MX. When repositioning a pa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1795-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-06-05 |
| Published | 2013-07-31 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Axiom Aristos MX Solid State Flat Panel Digital Imager, Model number 5895003. The device is used for diagnostic X-ray imaging.
Reason
Siemens issued a Field Safety Notice about the potential hazard to patients or operators when using the function "table top float" of the AXIOM Aristos MX. When repositioning a patient lying on the table top and releasing the table top, it is possible that the fingers of the patient or operator are between the table top and the detector tray and if the table top is moved, the fingers can be squee
Identifiers
| code_info | Model Number 5895003 with serial numbers 1052 through 2500. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1795-2013%22
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