FDA Device recall Z-2059-2015
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107
- FDA Device
- Class II
- terminated
- Published 2015-07-22
On 2015-07-22 the FDA classified a Class II recall of Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107 by Exactech, citing incorrect thread form on the screw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2059-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2009-03-06 |
| Published | 2015-07-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Exactech |
| Distribution | FL, GA, IL, NY, TX, WA |
Product
Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization and stabilization of spinal segments.
Reason
Incorrect thread form on the screw.
Identifiers
| code_info | Catalog Number 28202, Lot Number AS05107 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2059-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.