Exactech Optetrak Logic CC 15mm Tibial Augment Screws — Class II medical device recall Z-2704-2017
Terminated recall by Exactech, Inc., reported 2017-07-19, distributed in CA, NY. Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per ca
| Recall number | Z-2704-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2017-04-07 |
| Classified | 2017-07-08 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2020-08-04 |
| Distributed | CA, NY |
| Quantity | 9 devices |
| Serial numbers | 4739530, 4739531, 4739532, 4739533, 4739534, 4739535, 4739536, 4739537, 4739538 |
| Model numbers | 02-012-50-9015 |
Product
Exactech Optetrak Logic CC 15mm Tibial Augment Screws
Reason for recall
Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2704-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.