Hello all, The Medicines and Healthcare Products Regulatory Agency, (MHRA) have issued the following: Medical Device Alert MDA/2019/027 Issued: 25 July 2019 at 14:00 Automated external defibrillators: All Telefunken HR1 & FA1 – no valid CE certificate . The key information is as follows with the whole document, which is also attached. Manufactured by Defiteq International BV or GGT Holding BV – the safety and performance of these devices cannot be verified and their safe use can no longer be assured. Action • Initiate a process for sourcing an alternative defibrillator as these devices do not meet regulatory requirements for safety and performance. • Complete a local risk assessment for the continued use of the affected devices until an alternative device is sourced. • Report suspected or actual adverse events involving these devices through your local incident reporting system and/or your national incident reporting authorit...