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SCORPIO PATELLA ASSEMBLY INSTRUMENT (2016-08-02)
- Starting date:
- August 2, 2016
- Posting 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:
- Healthcare Professionals, General Public, Hospitals
- Identification number:
- RA-59878
Affected products
A. SCORPIO PATELLA ASSEMBLY INSTRUMENT
Reason
Stryker Orthopaedics has received reports of disassociated components of the Scorpio Patella Assembly instrument. An investigation revealed that the press-fit specifications between the pin(s) and either one or both clamping subcomponents were not met.
Affected products
A. SCORPIO PATELLA ASSEMBLY INSTRUMENT
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
3182-1000
Companies
- Manufacturer
-
Howmedica Osteonics Corporation
325 Corporate Drive
Mahwah
New Jersey
UNITED STATES