FDA Device recall Z-1226-2019
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x2…
- FDA Device
- Class II
- terminated
- Published 2019-05-08
On 2019-05-08 the FDA classified a Class II recall of Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x2… by Depuy Spine, citing A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1226-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-08 |
| Published | 2019-05-08 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Depuy Spine |
| Distribution | US |
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
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
Identifiers
| code_info | All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Depuy Spine
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FDA Device · Class II · 2022-07-13 · Depuy Spine - EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion i…
FDA Device · Class II · 2022-07-13 · Depuy Spine - Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (1…
FDA Device · Class II · 2019-05-08 · Depuy Spine - Confidence Plus Kit Spinal Cement System, Product Codes: 283910000 (GTIN: (01)10705034209623) and 283910000 (GTIN: (01)10705034209630) The…
FDA Device · Class II · 2018-04-11 · Depuy Spine - DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 26mm Item Code: 186852026 The SKYLINE¿ Anterior Cervic…
FDA Device · Class II · 2016-11-30 · Depuy Spine
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1226-2019%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.