PlainRecalls
FDA Devices Moderate Class II Terminated

120 V Neptune 3 Rover, Model Number: 0703-001-000

Reported: August 31, 2016 Initiated: July 1, 2016 #Z-2630-2016

Product Description

120 V Neptune 3 Rover, Model Number: 0703-001-000

Reason for Recall

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.

Details

Units Affected
78
Distribution
Domestic:MI, CA, ID, IA VA/DOD: None Foreign: None
Location
Portage, MI

Frequently Asked Questions

What product was recalled?
120 V Neptune 3 Rover, Model Number: 0703-001-000. Recalled by Stryker Instruments Div. of Stryker Corporation. Units affected: 78.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 31, 2016. Severity: Moderate. Recall number: Z-2630-2016.