Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
Panther and Panther Fusion Systems with 19-in monitorProduct code: 902615Serial Nos: 2090002307 to 2090002532Manufactured between April 2017 and Nov 2017ARTG Number: 260039 (Gen-Probe Australia Pty Ltd - Instrument/analyser IVDs)