Drug RecallsUpdate: Certain Philips Respironics Ventilators, BiPAP, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication Posted on by Editor Date: 03/14/2022 Product type: Medical Device USA-FDA link: https://www.fda.gov/medical-devices/safety-communications/update-certain-philips-respironics-ventilators-bipap-and-cpap-machines-recalled-due-potential-health https://templarpharma.com/fda-warns-against-use-of-renuvion-j-plasma-device-for-certain-aesthetic-procedures-fda-safety-communication/ ACON Laboratories Issues a Recall of Non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market
