FDA Device recall Z-0694-2019
Ingenia Elition S, Ingenia Elition X
- FDA Device
- Class II
- terminated
- Published 2019-01-16
On 2019-01-16 the FDA classified a Class II recall of Ingenia Elition S, Ingenia Elition X by Philips Medical Systems Nederlands, citing during automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0694-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-03 |
| Published | 2019-01-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips Medical Systems Nederlands |
| Distribution | CA, MN, NJ, NY, OH, TN, TX |
Product
Ingenia Elition S, Ingenia Elition X
Reason
During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
Identifiers
| code_info | Software version R5.5.0 Serial numbers: 45027 45011 45010 45024 45032 45026 45054 45035 45051 45052 45007…Software version R5.5.0 Serial numbers: 45027 45011 45010 45024 45032 45026 45054 45035 45051 45052 45007 45043 45044 45031 45039 45025 46001 45033 45050 45034 45049 45037 45048 46004 45046 45008 45058 45028 45029 45030 45042 46005 46011 45040 45045 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0694-2019%22
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