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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96831

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

Open FDA event record

Event summary

Timeline bucket
April 23, 2025
Product types
Device
Classifications
Class II
Statuses
Completed
Recalling firm wording
VIRTUAL INCISION CORPORATION

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

MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3

Z-1905-2025
Recall number
Z-1905-2025
Initiated
April 23, 2025
Classification
Class II
Status
Completed
Quantity
3 units

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
Software Version 4.0.3 loaded on the Surgeon Control Console 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

The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential to exhibit interrupted motion on the display screen, caused by a software latency between the movement of the hand controllers and the movement of the Surgical Minibot arms.

Code information

UDI-DI (01)00850038042028; Lot Numbers: 1020040211, 1020040212, 1020040213

Distribution pattern

US Distribution to States: CA, FL, NE