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.
Randox Liquid Cardiac Controls when used with CKMB and Myoglobin assays. An in vitro diagnostic medical device (IVD)Liquid Cardiac Control 1Catalogue Number: CQ5051Batch Numbers: 3909CK, 3913CK (exp. 28 Oct 2017), 3987CK (exp. 28 Apr 2018)Liquid Cardiac Control 2Catalogue Number: CQ5052Batch Numbers: 3911CK (exp. 28 Oct 2017), 3991CK (exp. 28 Apr 2018)Liquid Cardiac Control 3Catalogue Number: CQ5053Batch Numbers: 3912CK (exp. 28 Oct 2017)ARTG Number: 208141