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FDAApril 8, 2019device

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

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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