This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

PT Hybrid Glenoid Post

Starting date:
December 6, 2012
Posting date:
December 24, 2012
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-25935

Recalled Products

  1. PT Hybrid Glenoid Post

Reason

There is difficulty or inability to thread the PT Hybrid Glenoid Post to the glenoid base. The male thread of the post may be oversized.

Affected products

A. PT Hybrid Glenoid Post

Lot or serial number
  • 984850
  • 984800
Model or catalog number

PT-113950

Companies
Manufacturer
Biomet Orthopedics