FDA Device recall Z-1495-2020
Artis Q Biplane, Model No. 10848282
- FDA Device
- Class II
- terminated
- Published 2020-03-25
On 2020-03-25 the FDA classified a Class II recall of Artis Q Biplane, Model No. 10848282 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-1495-2020 |
| 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 Q Biplane, Model No. 10848282; Artis Q Ceiling, Model No.10848281; Artis Q Floor, Model No. 10848280; Artis Q zeego, Model No. 10848283 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: 117316 109490 117021 121396 121185 121430 117012 121406 109141 109502 109123 121336 109400…Serial numbers: 117316 109490 117021 121396 121185 121430 117012 121406 109141 109502 109123 121336 109400 109210 121089 109080 103061 109190 109191 109197 109198 121013 117136 117324 109418 109419 109421 121040 109405 109437 109119 109346 121445 121082 109460 121459 121011 109137 109512 117108 109300 121371 109187 121134 121374 109228 109412 109066 109067 109068 121053 121054 121422 117001 117023 109133 109134 121014 121112 121209 121325 109365 109217 109366 121357 109203 121051 109496 117330 109367 121402 103258 109542 121004 121167 121378 117329 121369 117315 121133 121163 121364 109202 121018 121154 121351 121354 117125 121418 121442 121151 121036 109500 117006 109451 121205 121340 121365 121137 109526 103013 109431 109383 121078 103053 121216 103035 109015 109136 117312 109132 117018 117124 109211 109144 109413 109482 109332 121381 109536 121457 121460 121352 |
|---|
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-1495-2020%22
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