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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75606

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

Open FDA event record

Event summary

Timeline bucket
November 01, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
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

3 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 3

Artis Q, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis zee / zeego and Q/ Q.zen include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee / zeego and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.

Z-0601-2017
Recall number
Z-0601-2017
Initiated
November 01, 2016
Classification
Class II
Status
Terminated
Quantity
4,657 systems (worldwide)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software in the Use Environment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

Code information

Model Numbers: 10848280, 10848281, 10848282, 10848283, 10848353, 10848354, 10848355

Distribution pattern

US Nationwide Distribution.

device · product 2 of 3

Artis zee/zeego, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis zee / zeego and Q/ Q.zen include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee / zeego and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.

Z-0602-2017
Recall number
Z-0602-2017
Initiated
November 01, 2016
Classification
Class II
Status
Terminated
Quantity
4,657 systems Worldwide

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software in the Use Environment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

Code information

Model Numbers: 10094135, 10094137, 10094139, 10094141, 10280959

Distribution pattern

US Nationwide Distribution.

device · product 3 of 3

AXIOM Artis, Angiographic x-ray system Product Usage: The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis zee / zeego and Q/ Q.zen include cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee / zeego and Q/ Q.zen can also support the acquisition of position triggered imaging for spatial data synthesis.

Z-0603-2017
Recall number
Z-0603-2017
Initiated
November 01, 2016
Classification
Class II
Status
Terminated
Quantity
4,657 systems Worldwide

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software in the Use Environment

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The possibility exists that the semi-automatic focus switch may not work as intended when pressing the footswitch multiple times.

Code information

Model Numbers: 5917054, 7008605, 7412807, 7413078, 7555357, 7555365, 7555373, 7727717, 7728392

Distribution pattern

US Nationwide Distribution.