medical Class II Updated 2019-05-08

DePuy Spine, Inc. recalls Concorde Lift, Expandable Interbody Device, spinal fusion im

Recalled Product

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

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All lots
View official government recall

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