Medical device recalls Moderate risk

Tosoh Smd Inc recalls Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as m…

Recall date
December 22, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1245-2017
FDA classification
Class II
Brand / firm
Tosoh Smd Inc
Sold / distributed
US Nationwide Distribution in the states of CT, MA, ME, MN, MO, NC, NE, NH, PA, SD, TX, VA, & WV.

Why it was recalled

Power outages causes reporting software to shutdown.

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

What was recalled

Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as middle ware between the Tosoh Automated HPLC G8 analyzer and an LIS or as a stand alone data repository for the analyzer. It is designed to store and manage the received data and make reports as necessary. The application is installed on Dell All- in-One computers that do not have serial (RS232) ports only USB ports. The G8 analyzer does not have USB ports. The Key Span Adaptor connects the serial port on the G8 to the USB port on the Dell computer. Once installed the Keyspan adapter is assigned a COM port. The default for the firmware is dynamic which randomly assigns a port for the transmission of data. The port assignment can change when the power for the analyzer or computer is shut down or the cable is physically disconnected and then reconnected. The default can be changed to geographic which allows the port assignment to be static regardless of a power outage.

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