Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Stryker NAV3i Platform is a mobile cart platform consisting Recalled by Stryker Instruments Div. of Stryker Corporation Due to The Stryker NAV3i Platform Power Boxes produced between...
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 Div. of Stryker Corporation directly.
Affected Products
The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera, SPC-3 Computer and IO-Tablet (touch screen) as well as the monitor, articulated arms and cart housing. This Navigation system is used in combination with surgical software for cranial, spine, ENT, orthopedic and trauma procedures.
Quantity: 20
Why Was This Recalled?
The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and March 7, 2014 may have been assembled without electrical insulation of the soldering joints
Where Was This Sold?
This product was distributed to 10 states: AR, CA, IN, LA, MD, MA, MI, MT, NV, TX
About Stryker Instruments Div. of Stryker Corporation
Stryker Instruments Div. of Stryker Corporation has 161 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report