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Stryker Instruments Div. of Stryker Corporation recalls 120 V Neptune 3 Rover, Model Number: 0703-001-000
Recalled August 31, 2016 · FDA recall Z-2630-2016 · Stryker Instruments Div. of Stryker
Hazard
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. · FDA Class II
Units
78
Sold at
Domestic:MI, CA, ID, IA VA/DOD: None Foreign: None
Description
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.
Product
120 V Neptune 3 Rover, Model Number: 0703-001-000
Manufacturer(s)
Stryker Instruments Div. of Stryker Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →