FDA Device recall Z-1468-2017
Axiom Artis fluoroscopic x-ray system
- FDA Device
- Class II
- terminated
- Published 2017-03-22
On 2017-03-22 the FDA classified a Class II recall of Axiom Artis fluoroscopic x-ray system by Siemens Medical Solutions Usa, citing A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1468-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-27 |
| Published | 2017-03-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
Axiom Artis fluoroscopic x-ray system
Reason
A gap in the housing of the wireless foot switch could potentially result in liquids penetrating the interior. Such liquids may include disinfectants, cleaning agents and/ or bodily fluids. In rare cases, the introduction of liquids in the wireless foot switch housing could result in the failure of the foot switch.
Identifiers
| code_info | Device Model: 4787813 Serial Numbers: 15260 20888 1104 20249 15197 10252 20019 20613 15508 10234 20425 2114…Device Model: 4787813 Serial Numbers: 15260 20888 1104 20249 15197 10252 20019 20613 15508 10234 20425 21143 22191 20124 20369 20681 22147 21346 1260 10127 10107 10100 15238 20128 21959 21966 21217 1204 21419 20721 21235 22085 1129 20627 20637 1294 1295 20240 21439 20715 1444 20983 22439 20171 1085 21885 1119 17109 15692 1065 17227 17223 21622 10008 10094 20432 21722 1801 22421 10275 10462 20134 1673 15126 15152 20521 21887 21448 20131 22038 21710 20723 1356 1347 10006 17174 10115 22103 22154 17050 21006 20381 15028 15518 22344 21095 20693 20801 20802 20394 1279 10059 10084 15268 21857 20349 21000 1196 15291 20000 22113 15432 20923 20829 17182 17110 21913 21954 22150 17073 17160 20200 21823 20567 17099 21291 20420 20976 20399 1262 150099 20183 21564 20281 10451 15393 20684 20423 20083 20503 21025 20130 22098 15330 15079 20349 21810 21811 21850 2186 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1468-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.