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Health product recall

Vanguard M Uni Tibial Trial (2015-04-22)

Starting date:
April 22, 2015
Posting date:
May 26, 2015
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-53491

Recalled Products

A. Vanguard M Uni Tibial  Trial

Reason

Biomet has initiated this action following an investigation which identified that the handle is incorrectly etched.

Affected products

A. Vanguard M Uni Tibial  Trial

Lot or serial number

70420

Model or catalog number
  • 32-423101
  • 32-423102
  • 32-423107
  • 32-423108
  • 32-423109
Companies
Manufacturer

Biomet Orthopedics

56 East Bell Drive

Warsaw

46581

Indiana

UNITED STATES