Boston Scientific Encore Advantage Kit, Material Numbers (UPN): 1. H74904527011; 2. H749045...

FDA Recall #Z-2534-2025 — Class II — August 5, 2025

Recall #Z-2534-2025 Date: August 5, 2025 Classification: Class II Status: Ongoing

Product Description

Boston Scientific Encore Advantage Kit, Material Numbers (UPN): 1. H74904527011; 2. H74904527052. (Interventional Cardiology and Peripheral Interventions)

Reason for Recall

The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that during use, foreign material particles could migrate from affected Encore 26 Inflation Devices into a balloon dilatation catheter.

Recalling Firm

Boston Scientific Corporation — Maple Grove, MN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

68347 units

Distribution

Worldwide distribution.

Code Information

1. H74904527011, GTIN 08714729180005, Lot Numbers: 34783060, 34849364, 34873499, 34942522, 34976509, 35017763, 35065979, 35067000; 2. H74904527052, GTIN 08714729127048, Lot Numbers: 34873681, 34915075, 34942524, 34986473, 34986475.

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated