FDA Device recall Z-2303-2018
Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures
- FDA Device
- Class II
- terminated
- Published 2018-07-04
On 2018-07-04 the FDA classified a Class II recall of Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures by Siemens Medical Solutions Usa, citing after the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2303-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-01 |
| Published | 2018-07-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures.
Reason
After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system.
Identifiers
| code_info | 121004 121019 121016 121008 121023 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2303-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.