Catalog 314-13-23 — Class II medical device recall Z-0459-2021
Terminated recall by Exactech, Inc., reported 2020-11-25, distributed in AZ, CA, CO, FL, IL, IN, KY, LA…. The product may be mislabeled.
| Recall number | Z-0459-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2020-10-06 |
| Classified | 2020-11-17 |
| Reported by FDA | 2020-11-25 |
| Terminated | 2023-11-13 |
| Distributed | AZ, CA, CO, FL, IL, IN, KY, LA, MD, ME, MN, NV, NY, OH, OK, SC, TN, TX, VA, WA, WI |
| Countries outside the US | AU, GB, JP |
| Quantity | 69 devices |
| Reason classes | labeling |
| Serial numbers | 6130334, 6130335, 6130336, 6130340, 6130341, 6130343, 6130344, 6130347, 6130352, 6130353, 6130355, 6130356, 6130357, 6130358, 6130361, 6130365, 6130366, 6130367, 6130368, 6142776, 6142777, 6142779, 6142780, 6142782, 6142783 and 43 more |
| Model numbers | 314-13-23 |
Product
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Reason for recall
The product may be mislabeled.
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-0459-2021. 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.