Concorde Lift — Class II medical device recall Z-1226-2019
Terminated recall by DePuy Spine, Inc., reported 2019-05-08, distributed nationwide. A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
| Recall number | Z-1226-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Spine, Inc., Raynham, MA, United States |
| Recall initiated | 2019-04-08 |
| Classified | 2019-04-26 |
| Reported by FDA | 2019-05-08 |
| Terminated | 2023-01-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, CH, GB |
| Quantity | 3,166 total |
Product
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)
Reason for recall
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
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-1226-2019. 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.