Health product recall

Modular Cathcart Fracture Head

Last updated

Summary

Product
Modular Cathcart Fracture Head
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Modular Cathcart Fracture Head Hip Ball (Endoprosthesis) All lots. 1363-43-000 1363-46-000 1363-50-000 1363-53-000 1363-44-000 1363-51-000 1363-48-000 1363-49-000 1363-42-000 1363-45-000 1363-47-000 1363-60-000 1363-58-000 1363-54-000 1363-41-000 1363-52-000 1363-56-000
Modular Cathcart Fracture Head Tapered Spacer Articul-Eze Taper (Endopros.) All lots. 1363-14-000

Issue

During an internal review, it was determined that the Cathcart head includes a +5mm offset, which was not specified in previous versions of the self-centering bipolar and Modular Cathcart unipolar endo heads surgical technique guide (stg). This +5mm offset should be taken into consideration when using a Cathcart head in a construct for hip arthroplasty procedures.

Recall start date: June 7, 2022

Additional information

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

Depuy Orthopaedics, Inc.

700 Orthopaedic Drive, Warsaw, Indiana, United States, 46582

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64293

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