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INTEGRAL CENTRALIZER LATERALIZED FEMORAL (2015-11-19)
- Starting date:
- November 19, 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-56198
Affected Products
INTEGRAL CENTRALIZER LATERALIZED FEMORAL
Reason
Zimmer Biomet has initiated this action following an investigation which identified that poly(methyl methacrylate) (PMMA) is listed as a material on the label but the product does not contain PMMA.
Affected products
INTEGRAL CENTRALIZER LATERALIZED FEMORAL
Lot or serial number
- 487400
- 505030
- 767120
Model or catalog number
- 11-162709
- 11-162711
Companies
- Manufacturer
-
Biomet Orthopedics
56 East Bell Drive
Warsaw
46581
Indiana
UNITED STATES