Stryker has identified a potential nonconformance for five lots of Smart Toe II implants (three of which have been imported into Canada). Specifically, the nickel-sensitivity statement on the outer carton may be partially covered by a label resulting in the statement showing "indicated for patients with nickel sensitivity" instead of "not indicated for patients with nickel sensitivity". The issue is detectable. The contraindications are clearly stated and visible in the instructions for use (IFU). Recall start date: Mar 30, 2022
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