SpineNet Anterior Cervical Cage — Class II medical device recall Z-2103-2013
Terminated recall by SpineNet, reported 2013-09-04, distributed nationwide. The recall decision has been made because because it has recently been determined that the instructions for us
| Recall number | Z-2103-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SpineNet, Winter Park, FL, United States |
| Recall initiated | 2013-02-05 |
| Classified | 2013-08-27 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2014-05-02 |
| Distributed | Nationwide (US) |
| Quantity | 400 |
| Model numbers | CL1012-05, CL1012-06, CL1012-07, CL1012-08, CL1012-09, CL1012-10, CL1014-05, CL1014-06, CL1014-07, CL1014-08, CL1014-09, CL1014-10 |
Product
SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in skeletally mature patients with degenerative disc disease of the cervical spine with accompanying radicular symptoms at one disc level
Reason for recall
The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing.
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-2103-2013. 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.