Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker USB Converter Recalled by Mako Surgical Corporation Due to Certain units have the potential to exhibit infant...
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 Mako Surgical Corporation directly.
Affected Products
Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery System.
Quantity: 2
Why Was This Recalled?
Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
Where Was This Sold?
This product was distributed to 2 states: AZ, IL
About Mako Surgical Corporation
Mako Surgical Corporation has 27 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report