Recall of NuVasive MAGEC 2 spinal rods with specific lot numbers due to risk of internal component separation after implantation, potentially causing tissue discoloration.
Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
NuVasive is recalling specific models of MAGEC 2 spinal rods that may separate after implantation, leading to titanium debris and tissue discoloration. This is a post-surgical issue requiring attention from users who have the affected products.
The actuator end cap component may separate after implantation, exposing internal parts that could cause titanium alloy wear debris to enter surrounding tissue, resulting in localized discoloration.
Surgical patients who received the recalled MAGEC 2 spinal rods during procedures between 2019 and 2023. The risk is primarily for those with the specific lot numbers listed in the recall.
Check the product label for the specific part numbers (MC2-4570R, MC2-4570S, etc.) and lot numbers listed in the recall. These products are surgical implants used in spinal procedures.
Reach out to NuVasive directly to confirm if your specific product is affected and to get instructions for next steps.
NuVasive is recalling specific models of MAGEC 2 spinal rods that may separate after implantation, potentially causing titanium debris and tissue discoloration.
Check the product label for the specific part numbers (MC2-4570R, MC2-4570S, etc.) and lot numbers listed in the recall.
The recall does not specify removal; it requires contacting NuVasive to determine if your product is affected.
We’ve drafted a message you can send NuVasive to request your refund or repair — edit it as you like.
Subject: Recall Z-1898-2020 — NuVasive NuVasive Hello, I own a NuVasive that is covered by recall Z-1898-2020 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.
