LFIT CoCr V40 Head and Femoral Head COCR LFIT (2018-05-24)
- Starting date:
- May 24, 2018
- Posting date:
- June 1, 2018
- 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-66954
Affected products
A. LFIT CoCr V40 Head
B. Femoral Head COCR LFIT
Reason
Stryker has received a higher than expected number of complaints documenting femoral head/hip stem dissociation for certain sizes of lfit? Anatomic CoCr V40TM Femoral Heads manufactured prior to march 4, 2011.
Affected products
A. LFIT CoCr V40 Head
Lot or serial number
More than 100 numbers, contact manufacturer.
Model or catalog number
6260-9-040
6260-9-044
6260-9-140
6260-9-144
Companies
- Manufacturer
-
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
07430
New Jersey
UNITED STATES
B. Femoral Head COCR LFIT
Lot or serial number
More than 100 numbers, contact manufacturer.
Model or catalog number
6260-9-036
6260-9-136
6260-9-236
6260-9-336
Companies
- Manufacturer
-
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
07430
New Jersey
UNITED STATES