DePuy Spine recalls Concorde Lift spinal fusion implants due to reported post-operative loss of height and migration. Affected models include 9x23, 9x27, 11x23, 11x27. Contact for details.
A complaint trend was observed for post-operative loss of height and migration for Concorde Lift G3+ implants.
DePuy Spine is recalling certain spinal fusion implants called Concorde Lift G3+ models because they have been reported to cause loss of height and migration after surgery. This could lead to complications requiring additional medical procedures.
The implants have been reported to lose height and migrate after surgery, meaning they may shift position in the spine. This can cause complications that might require additional surgical interventions to correct.
Patients who received the Concorde Lift G3+ spinal implants between 1978 and the present are likely affected. Those with recent spinal surgery using these specific models are at highest risk.
Check if your spinal implant has a model number like 9x23 (197809023L), 9x27 (197809027L), 11x23 (197811023L), or 11x27 (197811027L). These models were sold from 1978 onward.
Identify your spinal implant model number to confirm if it matches the recalled types (9x23, 9x27, 11x23, 11x27).
DePuy Spine recalls these implants due to reported post-operative loss of height and migration after surgery.
Check your implant model number to see if it matches the recalled types. Contact DePuy Spine for further guidance.
The implants have been reported to cause loss of height and migration after surgery, which may require additional medical procedures.
We’ve drafted a message you can send DePuy Spine to request your refund or repair — edit it as you like.
Subject: Recall Z-1226-2019 — DePuy Spine DePuy Spine Hello, I own a DePuy Spine that is covered by recall Z-1226-2019 from DePuy Spine. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
