medical Class II Updated 2019-05-08

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

Recalled Product

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

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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