FDA Device recall Z-1497-2020
Artis zee Biplane, Model No. 10094141
- FDA Device
- Class II
- terminated
- Published 2020-03-25
On 2020-03-25 the FDA classified a Class II recall of Artis zee Biplane, Model No. 10094141 by Siemens Medical Solutions Usa, citing A software issue could potentially cause the stand and table movements to be blocked.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1497-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-14 |
| Published | 2020-03-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Artis zee Biplane, Model No. 10094141; Artis zee Ceiling, Model No. 10094137; Artis zee Floor, Model No. 10094135; Artis zeego, Model No. 10280959 Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Reason
A software issue could potentially cause the stand and table movements to be blocked.
Identifiers
| code_info | Serial Numbers 154827 160851 148262 155168 154408 148299 137623 137714 125213 125238 125245 160869 147573…Serial Numbers 154827 160851 148262 155168 154408 148299 137623 137714 125213 125238 125245 160869 147573 126202 161046 161041 154454 153834 147581 147857 147562 154532 147983 161218 160999 161032 161204 125001 161226 147604 153890 154721 154722 137193 138055 147760 147923 160449 160834 160852 138035 160944 137479 146245 160994 154567 160959 147803 125249 125241 154704 160913 148260 138087 160886 148335 154086 138112 161206 147841 155189 154727 147954 147918 160877 161008 148250 160997 147558 160864 160845 160448 138147 147955 147957 147958 160965 160800 154509 147724 138102 161236 125222 147953 137388 147553 131219 160823 147736 148215 148216 147974 154792 148298 137766 148025 160431 147972 137595 160916 137335 148282 160814 160872 146323 147992 147601 147659 147894 148010 147905 160915 125229 137421 131221 147249 153743 161021 147500 147969 148270 137119 147936 |
|---|
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-1497-2020%22
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