Boston Scientific recalls AVVIGO+ Multi-Modality Guidance System with incorrect 9-grid overlay in Live mode when using OptiCross 18 catheter. This may cause inaccurate depth settings for peripheral vascular imaging.
Boston Scientific has received reports indicating the grid mark overlay on the cross-sectional view did not present correctly when an OptiCross 18 Peripheral Imaging Catheter was connected to the AVVIGO+ Multi-Modality Guidance System while in either Live or Record mode. The Boston Scientific investigation determined that, due to a software anomaly, a 9-grid mark overlay is incorrectly displayed during Live mode when AVVIGO+ is connected to an OptiCross 18 Peripheral Imaging Catheter. Note that the correct overlay display for this catheter is the 15-grid mark overlay, which allows for a reference depth setting of 14.9mm for peripheral catheters. This software anomaly is limited to Live or Record mode. In Review mode, the correct 15-grid mark overlay is displayed, and the vessel image is correctly scaled to the appropriate size.
Boston Scientific is recalling its AVVIGO+ Multi-Modality Guidance System because a software issue causes it to display a 9-grid overlay instead of the correct 15-grid overlay when used with an Opti:Cross 18 catheter in Live or Record mode. This could lead to inaccurate depth settings for peripheral vascular imaging, potentially affecting medical procedures.
The software anomaly causes the system to show a 9-grid overlay instead of the correct 15-grid overlay when connected to an OptiCross 18 catheter in Live or Record mode. This could result in inaccurate depth settings (14.9mm) for peripheral vascular imaging, potentially affecting procedure accuracy.
Physicians using the AVVIGO+ system with OptiCross 18 catheters in Live or Record mode. The risk is low as the issue only affects specific imaging modes and does not cause immediate harm.
The system uses Material Number H7492493220I0, GTIN/UDI/DI 00191506033255, and Batch/Serial Numbers 103900407 or 104650692. It is designed for medical imaging procedures with peripheral vascular catheters.
Verify if the system is in Live or Record mode when using an OptiCross 18 catheter.
Boston Scientific found a software anomaly causing the system to display a 9-grid overlay instead of the correct 15-grid overlay when connected to an OptiCross 18 catheter in Live or Record mode.
The risk is low as the issue only affects specific imaging modes and does not cause immediate harm. It could lead to inaccurate depth settings for peripheral vascular imaging.
The official recall does not provide a fix; the system correctly displays the 15-grid overlay in Review mode.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0099-2025 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0099-2025 from Boston Scientific. 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.
