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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91765

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

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Event summary

Timeline bucket
February 02, 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

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 systems with a Siemens Healthineers table or a Trumpf/ MAQUET table-A Fluoroscopic X-Ray system. Material # 10849000.

Z-1311-2023
Recall number
Z-1311-2023
Initiated
February 02, 2023
Classification
Class II
Status
Ongoing
Quantity
141 units US

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
In the event of any unintended table movement, the system may not detect the incorrect direction, could lead to the injury of a patient, staff member, operator, or equipment.

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

In the event of any unintended table movement, the system may not detect the incorrect direction, could lead to the injury of a patient, staff member, operator, or equipment.

Code information

UDI #: 4056869046877 Serial Numbers: 164011 164013 164018 164019 164021 164022 164024 164025 164026 164027 164028 164033 164034 164048 164049 164053 164054 164055 164057 164060 164061 164063 164064 164066 164068 164069 164071 164072 164073 164074 164075 164080 164083 164084 164086 164094 164095 164097 164098 164100 164105 164113 164115 164121 164124 164125 164134 164138 164140 164142 164152 164153 164155 164157 164158 164159 164160 164161 164163 164168 164171 164172 164173 164183 164184 164186 164187 164188 164189 164190 164196 164201 164202 164204 164205 164210 164211 164212 164213 164216 164227 164228 164231 164234 164240 164241 164242 164244 164250 164253 164263 164267 164269 164270 164275 164277 164279 164282 164287 164292 164293 164295 164297 164298 164299 164300 164303 164306 164311 164312 164315 164318 164319 164321 164322 164326 164328 164329 164330 164331 164332 164333 164338 164340 164344 164352 164353 164355 164359 164362 164366 164371 164377 164389 164391 164394 164397 164398 164399 164400 164403

Distribution pattern

US Nationwide distribution.