Stryker Instruments Div. of Stryker Corporation recalls 120 V Neptune 3 Rover, Model Number: 0703-001-000

Recall date

July 1, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2630-2016

FDA classification

Class II

Brand / firm

Stryker Instruments Div. of Stryker Corporation

Sold / distributed

Domestic:MI, CA, ID, IA VA/DOD: None Foreign: None

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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