FDA Device recall Z-2029-2019
Artis zee ceiling, Model Number 10094137
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of Artis zee ceiling, Model Number 10094137 by Siemens Medical Solutions Usa, citing A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the r….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2029-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-12 |
| Published | 2019-07-31 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Artis zee ceiling, Model Number 10094137
Reason
A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
Identifiers
| code_info | Serial Numbers: 146669 146877 146996 146663 147100 146286 146292 146410 146676 147155 147049 147233 146406…Serial Numbers: 146669 146877 146996 146663 147100 146286 146292 146410 146676 147155 147049 147233 146406 146407 146411 146121 146710 146945 147084 147189 147190 146679 146766 146232 146408 146409 146728 146335 146659 146993 146898 146965 146221 147273 146814 146871 146952 147030 147239 146988 146899 146368 146643 146650 146980 146361 146365 146366 146369 146912 147036 146116 146164 146168 147079 147371 146156 146342 146343 147129 146192 147081 146235 146201 146260 146277 146868 146758 146818 146741 146174 147507 146245 147047 125002 146171 146173 146176 146186 146187 146188 146189 147042 146630 146266 146305 146908 146267 147208 147247 146219 146272 146274 147096 125022 147236 146193 146761 147175 146298 146637 146972 147078 146976 146652 146327 146333 146338 147786 147023 146851 147249 147255 146688 146166 146144 147165 147188 146324 146715 146293 146308 146968 |
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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-2029-2019%22
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