Class II
Medical Device Recall: LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00
LINK BIO CORP · June 27, 2024
Reason for Recall
The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
Distribution
US Nationwide distribution in the states of FL, GA, KS, OH, WI.
States Affected
NATIONWIDE
Quantity Affected
8 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2445-2024
Status: ongoing
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