FDA Device recall Z-2449-2019
Proteus XR/a (SlOK : K993090)
- FDA Device
- Class II
- ongoing
- Published 2019-10-02
On 2019-10-02 the FDA classified a Class II recall of Proteus XR/a (SlOK : K993090) by Ge Healthcare, citing intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2449-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-08-09 |
| Published | 2019-10-02 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Proteus XR/a (SlOK : K993090)
Reason
Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.
Identifiers
| code_info | console part number 5441870) and (console spare part numbers 5462233, 5462233-R, 5761170, 5462233-H) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2449-2019%22
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