This morning (October 2nd, 2019) we were made aware of a product recall issued by the commonwealth Therapeutic Goods Administration for certain Philips defibrillators. While none of our clients appear to be affected by this recall, we feel it important to help spread the word .
This notice was issued on September 20th, 2019 and relates to FRx and HS1 defibrillators which may have an issue with printed circuit boards.
The information for the recall can be found on the attached PDF document or by going to tga.gov.au for more details.