This page has been archived on the Web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

TRIDENT UNIVERSAL IMPACTOR/POSITIONER

Starting date:
August 19, 2016
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-60084

Affected Products

TRIDENT UNIVERSAL IMPACTOR/POSITIONER

Reason

Manufacturer has received reports of the thread length protruding past the dome of the acetabular trial or implant. It was determined that the press fit between the threaded stud and the handle shaft assembly for the Trident Universal Impactor/Positioner (p/n: 2101-0200) may lead to the gradual protrusion of the threaded stud over time.

Affected products

TRIDENT UNIVERSAL IMPACTOR/POSITIONER

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

2101-0200

Companies
Manufacturer
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
New Jersey
UNITED STATES