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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 75383

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

Open FDA event record

Event summary

Timeline bucket
August 31, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Neusoft Medical Systems Co., Ltd.

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

NeuViz 64 Multi-slice CT Scanner Systems

Z-0875-2017
Recall number
Z-0875-2017
Initiated
August 31, 2016
Classification
Class II
Status
Terminated
Quantity
23 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Firm discovered during contrast agent tracking scan, when the expected concentration of contrast agent is reached, later planned scan may be interrupted. The system must be powered down and restarted to clear the interruption error before scanning can resume.

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

The Firm discovered during contrast agent tracking scan, when the expected concentration of contrast agent is reached, later planned scan may be interrupted. The system must be powered down and restarted to clear the interruption error before scanning can resume.

Code information

NeuViz 64e, NeuViz 64i with software version 1.0.6.3258 +P04 or previous version. NeuViz 64En, NeuViz 641n with software version 1.0.7.4021+P05 or previous version

Distribution pattern

US Distribution

device · product 2 of 2

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.7.4038+P06 or previous version

Z-0876-2017
Recall number
Z-0876-2017
Initiated
August 31, 2016
Classification
Class II
Status
Terminated
Quantity
23 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Firm discovered during contrast agent tracking scan, when the expected concentration of contrast agent is reached, later planned scan may be interrupted. The system must be powered down and restarted to clear the interruption error before scanning can resume.

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

The Firm discovered during contrast agent tracking scan, when the expected concentration of contrast agent is reached, later planned scan may be interrupted. The system must be powered down and restarted to clear the interruption error before scanning can resume.

Code information

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.7.4038+P06 or previous version

Distribution pattern

US Distribution