FDA Device recall Z-2704-2017
Exactech Optetrak Logic CC 15mm Tibial Augment Screws
- FDA Device
- Class II
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class II recall of Exactech Optetrak Logic CC 15mm Tibial Augment Screws by Exactech, citing missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2704-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-07 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Exactech |
| Distribution | CA, NY |
Product
Exactech Optetrak Logic CC 15mm Tibial Augment Screws
Reason
Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.
Identifiers
| code_info | Catalog No. 02-012-50-9015; Serial #'s 4739530, 4739531, 4739532, 4739533, 4739534, 4739535, 4739536, 4739537, and 4739538. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2704-2017%22
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