Altiva / Exactech Spine — Class II medical device recall Z-2059-2015
Terminated recall by Exactech, Inc., reported 2015-07-22, distributed in FL, GA, IL, NY, TX, WA. Incorrect thread form on the screw.
| Recall number | Z-2059-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2009-03-06 |
| Classified | 2015-07-10 |
| Reported by FDA | 2015-07-22 |
| Terminated | 2015-07-14 |
| Distributed | FL, GA, IL, NY, TX, WA |
| Quantity | 749 devices |
| Lot numbers | AS05107 |
| Model numbers | 28202 |
Product
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization and stabilization of spinal segments.
Reason for recall
Incorrect thread form on the screw.
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-2059-2015. 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.