FDA Device recall Z-2031-2019
Artis zee biplane, Model Number 10094141
- FDA Device
- Class II
- terminated
- Published 2019-07-31
On 2019-07-31 the FDA classified a Class II recall of Artis zee biplane, Model Number 10094141 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-2031-2019 |
| 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 biplane, Model Number 10094141
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: 153131 153229 153172 153315 153317 153992 153335 153695 153101 153102 153717 153779 153280…Serial Numbers: 153131 153229 153172 153315 153317 153992 153335 153695 153101 153102 153717 153779 153280 153648 153674 153166 153700 154096 153834 153194 153169 153803 153110 153890 154157 153199 153887 153269 154074 154012 153191 153252 153732 153239 154090 153227 153889 153655 153234 153236 153285 154686 153273 153251 153254 153344 154095 153342 154093 153171 153197 153916 153831 153256 153154 154086 153139 153882 153311 153211 153118 153987 153740 153863 153772 154079 153965 153707 154098 154073 153263 153276 154076 153758 131013 153257 154156 153351 153112 153155 153245 153318 153720 153998 153271 153857 153226 153939 153951 153290 153678 153679 153277 153125 153128 153134 153135 153743 153967 153946 153145 153866 153868 153829 153148 131021 153878 153906 153959 153709 153767 153217 153639 153119 153164 153304 153869 153719 153232 131005 153770 154020 153930 |
|---|
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-2031-2019%22
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