Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is a potential for the core diameter...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Instruments directly.
Affected Products
Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy procedures.
Quantity: 543
Why Was This Recalled?
There is a potential for the core diameter to be undersized, which may lead to the router breaking. A break can lead to unintended metal fragments in the surgical site, resulting in the potential for surgical intervention or damage to critical neurological or vascular structures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Instruments
Stryker Instruments has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report