Reported May 8, 2019 · Terminated
Concorde Lift, Lordotic Expandable Interbody Device, spinal fusion implant 9x23 (197809023L), 9x27 (197809027L), 11 x…
DePuy Spine, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: DePuy Spine, Inc. · 325 Paramount Dr · Raynham, MA · 02767-5199
Is this the product you have?
Concorde LiftLordotic Expandable Interbody Devicespinal fusion implant 9x23 (197809023L)9x27 (197809027L)11 x 23 (197811023L)11x27 (197811027L)9x23 (US197809023L)9x27 (US197809027L)
- Lot codes and dates
- All lots
- Amount recalled
- 3166 total
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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