Virtual Incision recalls MIRA Surgical System software version 4.0.3 due to potential display motion interruptions. Affected units have specific catalog numbers and lot numbers. Contact for remedy.
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.
Virtual Incision is recalling their MIRA Surgical System software version 4.0.3 because it may cause display motion interruptions. This could affect surgical procedures by making movements appear delayed or inconsistent on the screen.
The software may have a delay between hand movements and the surgical robot's response on the display screen. This could lead to inconsistent motion during surgery, but it does not cause physical harm or immediate danger.
Surgical teams using the MIRA Surgical System with software version 4.0.3 are affected. The risk is highest for medical professionals performing procedures with this specific software version.
Check for the catalog number MIRA-CAP-110 and software version 4.0.3. Affected units have lot numbers 1020040211, 1020040212, or 1020040213.
Verify the software version on the Surgeon Control Console. If it is 4.0.3, it may be affected.
The recall is for potential display motion interruptions, which could affect surgical procedures but does not cause physical harm or immediate danger.
Check the software version on your Surgeon Control Console. If it is 4.0.3, contact Virtual Incision for further instructions.
Affected units have catalog number MIRA-CAP-110 and software version 4.0.3 with lot numbers 1020040211, 1020040212, or 1020040213.
We’ve drafted a message you can send Virtual Incision to request your refund or repair — edit it as you like.
Subject: Recall Z-1905-2025 — Virtual Incision Virtual Incision Hello, I own a Virtual Incision that is covered by recall Z-1905-2025 from Virtual Incision. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
