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DePuy Spine, Inc. recalls Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23
Recalled May 8, 2019 · FDA recall Z-1226-2019 · 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, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x 23 (197811023L), 11x27 (197811027L), 9x23 (US197809023L), 9x27 (US197809027L)
Manufacturer(s)
DePuy Spine, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →