Smith & Nephew, Inc. recalls Genesis (GII) - Product Usage: designed for use in patients
Recalled Product
Genesis (GII) - Product Usage: designed for use in patients in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e. medial collateral and/or lateral collateral ligament) are absent or incompetent.
Hazard / Issue
The anterior locking detail does not meet its design specifications.
Issued by
FDA
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