Severity
Moderate
ModerateClass IICompleted
FDA Devices recall · Reported June 11, 2025
MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3
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 softw…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Virtual Incision Corporation recalled MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catal… - a moderate-severity action.
MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catal… was recalled by Virtual Incision Corporation in June 11, 2025. Reason: The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential …. Check the official notice for the remedy. Verify recall #Z-1905-2025 with the FDA Devices before acting.
The recall
Virtual Incision Corporation issued this moderate-severity FDA Devices recall-The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential ….
- Moderate
- severity level
- 3 units
- affected scope
- Class II
- classification
- June 11, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1905-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1905-2025) was formally reported on June 11, 2025, with the manufacturer initiating the action on April 23, 2025. It is classified under Moderate severity (Class II), with a current status of Completed. Virtual Incision Corporation is listed as the recalling firm, operating out of Lincoln, NE. Federal records list the affected scope as 3 units.
The documented reason for this recall is: 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 … Distribution data in the federal record shows the product reached: US Distribution to States: CA, FL, NE. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3 units
Related Recalls
6
3 from same agency
Product description
MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Completed |
| Recall number | Z-1905-2025 |
| Date reported | June 11, 2025 |
| Date initiated | April 23, 2025 |
| Recalling firm | Virtual Incision Corporation |
| Firm location | Lincoln, NE |
| Affected scope | 3 units |
| Distribution | US Distribution to States: CA, FL, NE |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1905-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3. Recalled by Virtual Incision Corporation. Units affected: 3 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 11, 2025. Severity: Moderate. Recall number: Z-1905-2025.
Where was the recalled product distributed? ▼
Distribution: US Distribution to States: CA, FL, NE.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1905-2025) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported June 11, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.