Cynch Lordotic T-PLlF Implant — Class II medical device recall Z-0932-2013
Terminated recall by Spine Smith Partners LP, reported 2013-03-20, distributed in TX. Implants were incorrectly laser marked as 23mm instead of 28mm.
| Recall number | Z-0932-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spine Smith Partners LP, Austin, TX, United States |
| Recall initiated | 2012-08-24 |
| Classified | 2013-03-10 |
| Reported by FDA | 2013-03-20 |
| Terminated | 2013-05-17 |
| Distributed | TX |
| Quantity | 3 units |
| NDC | 00609-2809-06 |
| Lot numbers | 39AQ |
| Model numbers | 0609-2809-06 |
Product
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Reason for recall
Implants were incorrectly laser marked as 23mm instead of 28mm.
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-0932-2013. 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.