NuVasive recalls X-Core 2 Ti Core implants used in spinal surgery due to potential inability to disengage from vertebral implants. Affected units have specific part numbers and lot codes. Consumers should contact NuVasive for details.
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
NuVasive is recalling X-Core 2 Ti Core spinal implants that may not disengage properly from the vertebrae. This could cause serious complications during surgery or after implantation if the device gets stuck. The recall affects specific model numbers and production lots.
The X-Core 2 Ti Core implant may not detach from the vertebrae replacement device during surgery or after implantation. If it gets stuck, it could cause complications like improper spinal alignment or the need for additional surgery to remove the device.
Spinal surgery patients who received the X-Core 2 Ti Core implant during procedures between 2019 and 2023 are likely affected. Patients with the specific part numbers and lot codes listed in the recall are at highest risk.
Check the product's part number and lot code on the packaging or device. Affected units have specific part numbers (7160012, 7160014, 7180016, 7180018, 7220016, 7220018) and corresponding lot numbers listed in the recall notice.
Identify the part number and lot code on the device or packaging to confirm if it's affected.
Yes, this recall affects patients who received the X-Core 2 Ti Core implant during spinal surgery between 2019 and 2023.
Check the part number and lot code on the device or packaging. Affected units have specific part numbers and lot codes listed in the recall notice.
Contact NuVasive directly to confirm if your implant is affected and get instructions for next steps.
We’ve drafted a message you can send NuVasive to request your refund or repair — edit it as you like.
Subject: Recall Z-0738-2023 — NuVasive NuVasive Hello, I own a NuVasive that is covered by recall Z-0738-2023 from NuVasive. 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.
