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LFIT COCR V40 and COCR LFIT Femoral Heads
- Starting date:
- August 24, 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-60268
Affected Products
- LFIT COCR V40 Head
- Femoral Head - COCR, LFIT
Reason
Stryker has received higher than expected complaints of taper lock failure for specific lots of certain sizes of LFIT Anatomic COCR V40TM Femoral Heads manufactured prior to 2011.
Affected products
A. LFIT COCR V40 Head
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
6260-9-240
6260-9-244
6260-9-340
6260-9-344
6260-9-440
6260-9-444
Companies
- Manufacturer
-
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
07430
UNITED STATES
B. Femoral Head - COCR, LFIT
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
6260-9-236
Companies
- Manufacturer
-
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
07430
UNITED STATES
- Date modified: