FDA Device recall Z-0710-2018
Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory by Siemens Medical Solutions Usa, citing the possibility exists for the wireless foot switch to fail due to impacts by external factors, such as electrostatic discharge that exceed a certain intensity. If the foot switch….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0710-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-09-28 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY |
Product
Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.
Reason
The possibility exists for the wireless foot switch to fail due to impacts by external factors, such as electrostatic discharge that exceed a certain intensity. If the foot switch fails, it will no longer be able to be used to release radiation. The hand switch provided can be used to release exposures; however, fluoroscopic examinations will not be possible.
Identifiers
| code_info | Serial Numbers: 10000 10006 10009 10010 10016 10018 10019 10027 10029 10030 10040 10042 10044 10046 10047…Serial Numbers: 10000 10006 10009 10010 10016 10018 10019 10027 10029 10030 10040 10042 10044 10046 10047 10048 10055 10056 10059 10062 10068 10069 10073 10075 10080 10084 10089 10094 10095 10096 10098 10099 10100 10102 10103 10104 10111 10112 10115 10116 10121 10122 10125 10126 10128 10133 1027 1049 1059 1072 1084 1085 1096 1101 1102 1104 1105 1111 1112 1115 1117 1122 1129 1131 1139 1144 1147 1149 1156 1157 1160 1165 1166 1182 1188 1189 1196 1199 1204 1205 1206 1208 1222 1227 1228 1229 1232 1233 1240 1242 1243 1245 1246 1248 1252 1255 1256 1258 1260 1262 1266 1267 1269 1270 1274 1278 1279 1282 1283 1286 1292 1293 1294 1295 1299 1300 13173 15000 15003 15004 15015 15016 15021 15024 15026 15028 15033 15034 15042 15045 15049 15053 15055 15056 15066 15069 15070 15074 15076 15079 15080 15087 15100 15103 15104 15105 15106 15108 15109 15111 1511 |
|---|
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-0710-2018%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.