Health product recall

Blueprint Mixed Reality Guidance Instrumentation System

Brand(s)
Last updated

Summary

Product
Blueprint Mixed Reality Guidance Instrumentation System
Issue
Medical devices - Performance
What to do

No impacted product has been distributed to Canadian customers. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Blueprint Mixed Reality BP MXR Depth Stop Pin

More than 10 numbers, contact manufacturer.

MRUE206

Blueprint Mixed Reality BP MXR Coracoid Clamp

23A362
22A976
22A544
23A008
23A364
23A365
23A363
22A543
22A975

MRUE202

Blueprint Mixed Reality Box Base

22B823
22B883
22B821
22B882
22B822
22B884
22B820

MRUE204

Blueprint Mixed Reality BP MXR Glenoid Digitizer

More than 10 numbers, contact manufacturer.

MRUE201

Blueprint Mixed Reality Glenoid Box Lid

22B824
22B827
22B825
22B886
22B826
22B885
22B887

MRUE205

Blueprint Mixed Reality BP MXR Glenoid Pin Guide

22C915
23A357
23B113
23B115
23B117
23A356
23B114
23B116
23B118
23A358

MRUE200

Blueprint Mixed Reality BP MXR Instrument Check Block

23A812
22C800
22A533
22A977

MRUE203

Issue

The nonconformance identified was that the overall complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation System was determined to have exceeded the anticipated complaint rate threshold.

Recall Start Date: February 24, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies

Tornier S.A.S.

161, Rue Lavoisier, Montbonnot-Saint-Martin, France, 38330

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77078

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