FDA Device recall Z-0104-2025
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO + MOB SYSTEM EU + ROW
- FDA Device
- Class II
- ongoing
- Published 2024-10-23
On 2024-10-23 the FDA classified a Class II recall of Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO + MOB SYSTEM EU + ROW by Boston Scientific, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0104-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-09-05 |
| Published | 2024-10-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Boston Scientific |
| Distribution | US |
Product
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO + MOB SYSTEM EU + ROW; the system utilizes an interactive display to provide physicians with physiologic, intravascular and/or intracardiac anatomical information. The system can provide various modalities which includes intravascular ultrasound (IVUS). When used with a peripheral vascular imaging catheter, the system utilizes the IVUS modality for ultrasound examination of intravascular pathology.
Reason
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.
Identifiers
| code_info | Material Number H7492493320C0, GTIN/UDI/DI 00191506033309, Batch/Serial Numbers: 103189853, 103416434, 103416437, 1034…Material Number H7492493320C0, GTIN/UDI/DI 00191506033309, Batch/Serial Numbers: 103189853, 103416434, 103416437, 103416600, 103416629, 103416630, 103416690, 103469208, 103552000, 103552353, 103645606, 103645607, 103667250, 103710560, 103711075, 103799547, 104033389, 104035234, 104042507, 104112099, 104112181, 104113877, 104119696, 104124626, 104124634, 104125281, 104125291, 104185271, 104185745, 104196585, 104210922, 104212968, 104338136, 104340593, 104523528, 104535237, 104535289, 104548777, 104573317, 104586006, 104586008, 104586060, 104596504, 104597121, 104597142, 104877669, 104884458, 104889669, 104890938, 104890985, 104902736, 105072735, 105092091, 105092230, 105092231, 105471081, 105491421, 105542133 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0104-2025%22
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