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DePuy Spine, Inc. recalls Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (19
Recalled May 8, 2019 · FDA recall Z-1225-2019 · DePuy Spine
Hazard
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants. · FDA Class II
Units
3166 total
Sold at
US Nationwide distribution. Foreign distribution to Austria, Switzerland, and United Kingdom.
Description
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
Product
Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (197811026C), 9x21 (US197809021C), 9x26 (US197809026C)
Manufacturer(s)
DePuy Spine, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →