CEZANNE II TLIF Bullet-Tip Cage — Class II medical device recall Z-2502-2020
Completed recall by CTL Medical Corporation, reported 2020-07-15, distributed in AZ, FL, IN, KS, MA, MI, NY, TN…. Reports received of the device fracturing during insertion.
| Recall number | Z-2502-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | CTL Medical Corporation, Addison, TX, United States |
| Recall initiated | 2019-08-21 |
| Classified | 2020-07-04 |
| Reported by FDA | 2020-07-15 |
| Distributed | AZ, FL, IN, KS, MA, MI, NY, TN, TX |
| Quantity | 39 units |
| Lot numbers | 14LEDODB, 15CNDOGC, 15DJDOEC |
| Model numbers | 018.1907 |
Product
CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.
Reason for recall
Reports received of the device fracturing during insertion.
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-2502-2020. 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.