Stryker recalls a specific neurosurgery bur model due to potential mismatch between package contents and outer label. This could lead to using the wrong device during surgery. Affected units include the 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) with GTIN 04546540362483.
There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-030 but package contains a 5820-107-530 device).
Stryker is recalling a specific neurosurgery bur model because the device inside the package might not match the product code on the outer label. Using the wrong bur could lead to incorrect surgical procedures.
The package may contain a different model number (e.g., 5820-107-530) than what's listed on the outer label. This mismatch could cause the wrong bur to be used during surgery, potentially leading to incorrect procedures.
Surgical professionals and hospitals that purchased the 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) with GTIN 04546540362483 are affected. The risk is low as the issue is a labeling mismatch, not a safety hazard.
Check the outer label for the model number (e.g., 5820-107-030). The product was sold with GTIN 04546540362483 and lot number 21341057.
Check the outer label for the model number (e.g., 5820-107-030) to ensure it matches the package contents.
The recall is due to potential mismatch between the device inside the package and the model number on the outer label, which could lead to using the wrong bur during surgery.
The correct model number is 5820-107-030, but the package may contain a different model (e.g., 5820-107-530).
Check the outer label for the model number (e.g., 5820-107-030) and the GTIN 04546540362483 with lot number 21341057.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0980-2025 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0980-2025 from Stryker. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
