Exactech, Inc. recalls Exactech Optetrak Logic CC 15mm Tibial Augment Screws
- Recall date
- April 7, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2704-2017
- FDA classification
- Class II
- Brand / firm
- Exactech, Inc.
- Sold / distributed
- CA and NY.
Why it was recalled
Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Exactech Optetrak Logic CC 15mm Tibial Augment Screws
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