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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93127

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 12, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Siemens Medical Solutions USA, Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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

Z-0195-2024
Recall number
Z-0195-2024
Initiated
September 12, 2023
Classification
Class II
Status
Ongoing
Quantity
237 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
Software issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

***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 42141 42146 42147 42148 42156 42160 42161 42185 42186 42187 42188 42189 42190 42191 42196 42199 42202 43000 43002 43003 43006 43007 43013 43022 43023 43025 43026 43027 43028 43029 43031 43033 43034 43037 43042 43044 43045 43046 43048 43049 43055 43058 43060 43061 43062 43063 43072 43073 43076 43079 43086 43095 43105 43106 43108 43112 43142 43143 43150 43161 43163 43177 43193 43208 43222 43226 43231 43257 43261 43279 43283 43286 43289 43291 43296 43297 43298 43319 43339

Distribution pattern

Nationwide

device · product 2 of 2

***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray System. Designed for the surgical environment and provides comprehensive image acquisition modes. Material Number: 11108110 (2)Cios Spin- a mobile x-ray system designed to provide x-ray imaging of the anatomical structures of patients during clinical applications Material Number: 10308194

Z-0196-2024
Recall number
Z-0196-2024
Initiated
September 12, 2023
Classification
Class II
Status
Ongoing
Quantity
***Updated 12/4/23*** 186 units Cios Flow, 181 units Cios Spin

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
Software issue

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

***Updated 12/4/23*** (1) UDI-DI: 04056869246628 S/N: 80006 80009 80010 80014 80017 80018 80019 80020 80021 80022 80023 80025 80026 80028 80031 80032 80033 80048 80051 80052 80053 80055 80059 80060 80063 80064 80065 80067 80068 80069 80071 80072 80073 80074 80075 80080 80081 82010 82011 82012 82013 82028 82031 82036 82037 82038 82039 82040 82043 82044 82045 82046 82061 82075 82076 82079 82080 82089 82092 82095 82096 82097 82112 82123 82124 82131 82132 82139 82144 82157 82159 82160 82161 82162 82163 82172 82176 82177 82178 82182 82183 82193 82194 82196 82198 82199 82200 82203 82205 82206 82207 82215 82223 82226 82227 82229 82236 82239 83003 83004 83005 83007 83008 83011 83012 83013 83023 83027 83029 83030 83034 83035 83038 83039 83040 83041 83048 83052 83053 83060 83063 83064 83070 83074 83086 83093 83094 83100 83102 83104 83108 83110 83112 83114 83115 83116 83117 83126 83128 83134 83138 83140 83141 83143 83144 83154 83155 83161 83194 83196 83220 83228 83229 83233 83245 83246 83247 83249 83273 83281 83283 83285 83303 83307 83311 83356 83357 83373 83374 83376 83412 83425 83441 83449 83454 83456 83458 83465 83473 83476 83490 83491 83493 83497 83514 83515 2) UDI-DI: 04056869153506 Serial: 50030 50032 50033 50048 50050 50051 50072 50073 50075 50079 50081 50088 50094 50096 50098 50101 50107 50109 50111 50120 50122 50123 50124 50127 50129 50130 50131 50132 50135 50153 50155 50166 50171 50184 50185 50192 50198 50199 50200 50201 50209 50210 50211 50213 50214 50215 50216 50219 50222 50276 50282 50302 50311 50315 50426 50427 50429 50431 50444 52008 52011 52018 52019 52022 52023 52024 52026 52027 52028 52029 52030 52034 52036 52037 52050 52070 52075 52078 52082 52088 52091 52093 52104 52108 52110 52111 52113 52116 52117 52121 52122 52124 52127 52130 52132 52137 52139 52140 52147 53006 53007 53008 53010 53011 53012 53014 53018 53024 53027 53030 53033 53035 53038 53039 53040 53042 53045 53047 53048 53049 53050 53053 53056 53057 53065 53067 53071 53072 53080 53087 53089 53095 53098 53099 53100 53102 53104 53105 53107 53108 53113 53117 53136 53153 53155 53156 53157 53158 53161 53163 53166 53168 53170 53172 53173 53174 53175 53178 53179 53181 53183 53185 53191 53194 53195 53198 53199 53200 53201 53202 53203 53205 53206 53207 53209 53210 53213 53214 53215 53218 53224

Distribution pattern

Nationwide