DePuy Spine, Inc.: Medical Device Recall in 2019 - (Recall #: Z-1226-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)

Product Classification:

Class II

Date Initiated: April 8, 2019

Date Posted: May 8, 2019

Recall Number: Z-1226-2019

Event ID: 82587

Reason for Recall:

A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.

Status: Terminated

Product Quantity: 3166 total

Code Information:

All lots

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated