Health product recall

Orise Proknife Procedure and Gel Syringe Kits

Last updated

Summary

Product
Orise Proknife Procedure and Gel Syringe Kits
Issue
Medical devices - Performance issue
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

Orise Proknife Procedure Kit

All lots.

M00519400
M00519380
M00519390

Orise Gel Syringe Single Pack

All lots.

M00519231
M00519221

Orise Gel Syringe Twin Pack

All lots.

M00519210
M00519211
M00519201

Issue

Boston Scientific recently became aware of events associated with foreign body reaction which presented as mass formations from remnant Orise gel post procedure, prompting unnecessary surgical intervention at a rate of 0.0019% of units sold (based on known events and total sales to date). There have been no reported deaths associated with these events. As a result of these events, updates will be made to the product IFUs. The purpose of the updates is to (a) raise awareness that remnant Orise gel may elicit a foreign body reaction with granuloma and multinucleate giant cells that can physically appear as mass formations and submucosal distortions, (b) provide new warnings and precautions, and (c) reinforce the existing procedural instructions and the need to document the use of Orise gel during the procedure. Boston scientific is not removing any Orise gel devices from the field; devices remain available for use.

Recall start date: October 11, 2022

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Health products - Medical devices - General hospital and personal use
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-72078

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