Health product recall

Encore™ 26 Inflation Device, Encore™ 26 Advantage kits, NephroMax™ kits and UroMax Ultra™ kits

Last updated

Summary

Product
Encore™ 26 Inflation Device, Encore™ 26 Advantage kits, NephroMax™ kits and UroMax Ultra™ kits
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalog number
UroMax Ultra™ Balloon Dilatation Catheter More than 50 numbers, contact manufacturer. M0062251230
UroMax Ultra™ Balloon Dilatation Catheter More than 50 numbers, contact manufacturer. M0062251260
UroMax Ultra™ Balloon Dilatation Catheter More than 50 numbers, contact manufacturer. M0062251200
UroMax Ultra™ Balloon Dilatation Catheter More than 50 numbers, contact manufacturer. M0062251210
Encore™ 26 Inflation Device More than 50 numbers, contact manufacturer. M0067101140
Encore™ 26 Inflation Device More than 50 numbers, contact manufacturer. M001151062
Encore™ 26 Inflation Device More than 50 numbers, contact manufacturer. M001151050
Encore™ 26 Inflation Device More than 50 numbers, contact manufacturer. M00566670
Encore™ 26 Advantage Kit More than 50 numbers, contact manufacturer. H74904527011
Encore™ 26 Advantage Kit More than 50 numbers, contact manufacturer. H74904527052
NephroMax™ High Pressure Nephrostomy Balloon Catheter More than 50 numbers, contact manufacturer. M0062101180
NephroMax™ High Pressure Nephrostomy Balloon Catheter More than 50 numbers, contact manufacturer. M0062101600

Issue

Boston Scientific is initiating a removal of certain batches of the Encore™ 26 Inflation Device and certain batches of Encore™ 26 Advantage kits, NephroMax™ kits and UroMax Ultra™ kits in which the impacted Encore™ 26 inflation devices are a component due to the potential presence of foreign material. 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.

Recall start date: August 5, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Gastroenterology and urology
Health products - Medical devices - Cardiovascular
Companies

Boston Scientific Corporation

300 Boston Scientific Way, Marlborough, Massachusetts, United States, 01752

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77906

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