FDA Device recall Z-0195-2024

Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200

FDA Device
Class II
ongoing
Published 2023-11-08

On 2023-11-08 the FDA classified a Class II recall of Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200 by Siemens Medical Solutions Usa, citing software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems, fulfillment of new requirements from DIN and IEC standards for Cios VA30 systems required may result in patie….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0195-2024
Classification	Class II
Status	ongoing
Initiated	2023-09-12
Published	2023-11-08
Last updated	2026-09-13 11:56 UTC
Company	Siemens Medical Solutions Usa
Distribution	US

Product

Siemens Cios Alpha (VA30) mobile fluoroscopic C-arm X-ray System, designed for the surgical environment. 11105200

Reason

Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems, fulfillment of new requirements from DIN and IEC standards for Cios VA30 systems required may result in patient misdiagnosis/repeat exposure

Identifiers

code_info	*Updated 12/4/23* UDI-DI: 04056869153490 S/N: 40013 40014 40015 40018 40020 40023 40030 40032 40033 40034 40035 40… *Updated 12/4/23* UDI-DI: 04056869153490 S/N: 40013 40014 40015 40018 40020 40023 40030 40032 40033 40034 40035 40036 40039 40040 40046 40047 40048 40049 40050 40051 40052 40054 40055 40057 40058 40062 40070 40073 40075 40076 40077 40078 40080 40083 40084 40093 40094 40095 40102 40103 40104 40107 40108 40109 40110 40111 40116 40117 40119 40121 40122 40123 40124 40125 40126 40130 40134 40135 40137 40139 40157 40158 40160 40161 40162 40163 40164 40167 40168 40169 40170 40171 40174 40175 40176 40188 40189 40190 40191 40192 40193 40194 40196 40206 40208 40215 40220 40226 40228 40230 40231 40234 40236 40238 40239 40240 40242 40244 40245 40246 40248 40250 40251 40252 40255 40256 40257 40259 40261 40263 40264 40265 40266 40267 40268 40270 40271 40273 40276 40314 40315 40317 40318 40322 40323 40324 40336 40339 42001 42002 42003 42004 42005 42006 42010 42018 42024 42025 42028 42032 42033 42037 42040 42041 42042 42045 42046 42052 42057 42061 42068 42069 42082 42087 42094 42101 42111 42140 4

code_info

***Updated 12/4/23*** UDI-DI: 04056869153490 S/N: 40013 40014 40015 40018 40020 40023 40030 40032 40033 40034 40035 40…

***Updated 12/4/23*** UDI-DI: 04056869153490 S/N: 40013 40014 40015 40018 40020 40023 40030 40032 40033 40034 40035 40036 40039 40040 40046 40047 40048 40049 40050 40051 40052 40054 40055 40057 40058 40062 40070 40073 40075 40076 40077 40078 40080 40083 40084 40093 40094 40095 40102 40103 40104 40107 40108 40109 40110 40111 40116 40117 40119 40121 40122 40123 40124 40125 40126 40130 40134 40135 40137 40139 40157 40158 40160 40161 40162 40163 40164 40167 40168 40169 40170 40171 40174 40175 40176 40188 40189 40190 40191 40192 40193 40194 40196 40206 40208 40215 40220 40226 40228 40230 40231 40234 40236 40238 40239 40240 40242 40244 40245 40246 40248 40250 40251 40252 40255 40256 40257 40259 40261 40263 40264 40265 40266 40267 40268 40270 40271 40273 40276 40314 40315 40317 40318 40322 40323 40324 40336 40339 42001 42002 42003 42004 42005 42006 42010 42018 42024 42025 42028 42032 42033 42037 42040 42041 42042 42045 42046 42052 42057 42061 42068 42069 42082 42087 42094 42101 42111 42140 4

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0195-2024%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.