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FDAApril 8, 2019device

Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (US197809026C)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

depuy spinedepuy

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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