The FDA revoked the emergency use authorizations for non-NIOSH-approved disposable respirators and the EUAs for decontamination and bioburden reduction systems.Link to original article Medtronic Recalls HeartWare HVAD System Batteries for Electrical Faults That Cause Battery Failure Certain Philips Respironics BiPAP Machines Recalled Due to a Plastic Issue: FDA Safety Communication Share Print Please login or register to post comments.