FDA Device recall Z-1895-2019
Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137
- FDA Device
- Class II
- terminated
- Published 2019-07-10
On 2019-07-10 the FDA classified a Class II recall of Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137 by Siemens Medical Solutions Usa, citing artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining th….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1895-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-06 |
| Published | 2019-07-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137
Reason
Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
Identifiers
| code_info | Serial Numbers: 147208 146637 146395 146728 146942 146697 146663 146731 146945 146774 146784 146866 147186…Serial Numbers: 147208 146637 146395 146728 146942 146697 146663 146731 146945 146774 146784 146866 147186 146867 146692 146869 146759 146776 146775 146797 146871 146801 146857 146803 146886 146758 146806 146851 146929 147157 146971 146919 146969 146973 146925 147695 146948 146964 147046 146861 147123 146883 147216 147866 146888 146955 147214 146921 147931 147100 146928 146946 147030 146983 146899 147089 146975 146963 146986 146960 146898 146937 146918 147047 146977 146993 147035 146982 147075 147084 146991 147114 147023 147233 147049 147036 147093 147009 147500 146996 147029 147174 147766 147113 147241 147083 147087 147124 147120 147119 147172 147692 147693 147775 147165 147167 147303 147079 147203 147107 147168 147144 147237 147240 147236 147239 147243 147234 147190 147175 147515 147559 147250 147254 147253 147252 147251 147649 147612 147557 147507 147516 147585 |
|---|
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-1895-2019%22
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