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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90904

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 20, 2022
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

1 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 1

ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000

Z-0119-2023
Recall number
Z-0119-2023
Initiated
September 20, 2022
Classification
Class II
Status
Ongoing
Quantity
140 US

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
software issues with ARTIS pheno systems with software version VE10B. This may

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

Siemens has become aware of three potential software issues with ARTIS pheno systems with software version VE10B. This may lead to a hazardous situation for patients if treatment cannot be continued on the system and treatment needs to be continued on an alternate system.

Code information

UDI-DI: 04056869046877 Serial No 164140 164138 164159 164331 164332 164033 164287 164282 164210 164183 164184 164311 164312 164328 164034 164391 164318 164244 164306 164155 164340 164189 164271 164277 164173 164292 164231 164095 164057 164054 164055 164132 164329 164072 164190 164048 164025 164026 164027 164338 164094 164241 164326 164267 164186 164068 164121 164157 164019 164152 164161 164013 164069 164213 164073 164257 164293 164263 164298 164060 164083 164113 164021 164066 164362 164398 164124 164125 164366 164279 164075 164074 164084 164086 164098 164153 164330 164389 164394 164172 164295 164353 164234 164321 164242 164270 164275 164315 164344 164163 164158 164053 164171 164297 164134 164253 164333 164188 164377 164063 164064 164397 164299 164300 164105 164160 164024 164080 164049 164240 164359 164227 164228 164018 164022 164250 164061 164187 164115 164399 164011 164204 164205 164211 164212 164216 164100 164097 164269 164303 164322 164400 164196 164355 164352 164168 164319 164201 164202 164371

Distribution pattern

Domestic distribution nationwide. Foreign distribution worldwide.