# FDA recall Z-1226-2019

> **DePuy Spine, Inc.** · Class II · device recall initiated 2019-04-08.

## 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.

## Distribution

US Nationwide distribution. Foreign distribution to Austria, Switzerland, and United Kingdom.

## Key facts

- **Recall number:** Z-1226-2019
- **Recalling firm:** DePuy Spine, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-08
- **Report date:** 2019-05-08
- **Termination date:** 2023-01-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raynham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1226-2019

## Citation

> AI Analytics. FDA recall Z-1226-2019. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1226-2019. Source: US FDA. Licensed CC0.

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