Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO II TO AVVIGO MOB UPGRADE US; 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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Material Number H7492493121C0, GTIN/UDI/DI 00191506033194, Batch/Serial Numbers: 102946988, 102946990, 102949556, 103199497, 103199500, 103199502, 103207815, 103207817, 103207860, 103439257, 103439962, 104233565, 104233569, 104233592, 104260813, 104278173, 104284141, 104322013, 104322062, 104322063, 104322064, 104322065, 104329117, 104329122, 104330747, 104330955, 104333933, 104340756, 104340852, 104340854, 104341075, 104350753, 104350860, 104350861, 104599296, 104599354, 104601145, 104601146, 104601151, 104601162
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Boston Scientific Corporation
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO II TO AVVIGO MOB UPGRADE US; 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.
Product Codes/Lot Numbers:
Material Number H7492493121C0, GTIN/UDI/DI 00191506033194, Batch/Serial Numbers: 102946988, 102946990, 102949556, 103199497, 103199500, 103199502, 103207815, 103207817, 103207860, 103439257, 103439962, 104233565, 104233569, 104233592, 104260813, 104278173, 104284141, 104322013, 104322062, 104322063, 104322064, 104322065, 104329117, 104329122, 104330747, 104330955, 104333933, 104340756, 104340852, 104340854, 104341075, 104350753, 104350860, 104350861, 104599296, 104599354, 104601145, 104601146, 104601151, 104601162
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0116-2025
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