FDA Device recall Z-1203-2023
Phoenix mKDR Xpress, digital mobile diagnostic x-ray system
- FDA Device
- Class II
- ongoing
- Published 2023-03-08
On 2023-03-08 the FDA classified a Class II recall of Phoenix mKDR Xpress, digital mobile diagnostic x-ray system by Sedecal, citing sedecal was informed of 3 incidents of erratic movements related to X-ray mobile systems.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1203-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-06 |
| Published | 2023-03-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Sedecal |
| Distribution | n/a |
Product
Phoenix mKDR Xpress, digital mobile diagnostic x-ray system
Reason
Sedecal was informed of 3 incidents of erratic movements related to X-ray mobile systems.
Identifiers
| code_info | UDI/DI 08436046003163, Serial Numbers: PH00202, PH00203, PH00204, PH00205, PH00206, PH00207, PH00208 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1203-2023%22
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