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Recall Observatory FDA recall evidence

Device product

Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO+ BRIDGE TO INTEGRATED KIT; 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.

Z-0095-2025

September 05, 2024

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 95331
Status
Ongoing
Classification
Class II
Quantity
9 units
Official record key
device-enforcement:Z-0095-2025

Official wording

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.

Code information: Material Number H7492493150I0, GTIN/UDI/DI 00191506033224, Batch/Serial Numbers: 102888346, 102888349, 103233723, 103233724, 104384572, 104399815, 104420529, 104618017, 104618220

Distribution pattern: US Nationwide distribution in Puerto Rico.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software anomaly