Stryker Neuro Match Head Soft Touch Bur Recall: Incorrect Model in Package
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.
Lower-risk recall
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).
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/57776-stryker-neuro-match-head-soft-touch-bur-recall-incorrect-model.
Source Summary by GovInfoNow · govinfonow.com/recall/57776-stryker-neuro-match-head-soft-touch-bur-recall-incorrect-model · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0980-2025
Cite this page
“Stryker Neuro Match Head Soft Touch Bur Recall: Incorrect Model in Package.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57776-stryker-neuro-match-head-soft-touch-bur-recall-incorrect-model. Based on FDA recall #Z-0980-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0980-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check the outer label for the model number (e.g., 5820-107-030). The product was sold with GTIN 04546540362483 and lot number 21341057.
- Brand
Stryker- Product
The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is intended to be used to cut bone and bone cement during- Category
Medical device
What to do — step by step
Verify Model Number
Check the outer label for the model number (e.g., 5820-107-030) to ensure it matches the package contents.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Colombia, Sweden, Netherlands, UK.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0980-2025 (June 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0980-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.