Health product recall

CPT Hip System Femoral Stem 12/14 Neck Taper

Brand(s)
Last updated

Summary

Product
CPT Hip System Femoral Stem 12/14 Neck Taper
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

CPT Hip System - Femoral Stem Neck Taper W/Centralizer

All lots.

00-8114-000-00
00-8114-000-10
00-8114-001-10
00-8114-003-00
00-8114-002-30
00-8114-003-30
00-8114-004-10
00-8114-002-00
00-8114-003-10
00-8114-003-18
00-8114-004-30
00-8114-002-18
00-8114-004-20
00-8114-004-23
00-8114-004-26
00-8114-005-00
00-8114-001-00
00-8114-002-10
00-8114-004-00
00-8114-005-10
00-8114-005-30

CPT Hip System - Stem, Small, Standard

All lots.

00-8114-050-00

CPT Hip System -Stem Valgus Neck Size Revision

All lots.

00-8114-013-18
00-8114-012-18

CPT Hip System - Stem, X-Small, Standard

All lots.

00-8114-040-00

Issue

Zimmer Biomet is voluntarily initiating a medical device field action correction for the CPT Hip System Femoral Stem 12/14 Neck Taper due to increased risk of postoperative periprosthetic femoral fracture (PFF).

Recall Start Date: July 8, 2024

Additional information

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

Zimmer Inc.

1800 West Center Street, Warsaw, Indiana, United States, 46580

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75835

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