Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
120 V Neptune 3 Rover Recalled by Stryker Instruments Div. of Stryker Corporation Due to Stryker initiated a voluntary recall of the 120...
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
120 V Neptune 3 Rover, Model Number: 0703-001-000
Quantity: 78
Why Was This Recalled?
Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016, due to a potential for the device to experience system errors causing the device to shutdown if high levels of electromagnetic interference are present in the operating room.
Where Was This Sold?
This product was distributed to 5 states: CA, ID, IA, MI, VA
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