Audit Flags Gaps in Medical Equipment Oversight, Maintenance in New York’s Emergency Stockpile
A state audit finds tens of thousands of ventilators and other devices purchased during COVID-19 remain unused and unmaintained.
A state audit finds tens of thousands of ventilators and other devices purchased during COVID-19 remain unused and unmaintained.
CorVent Medical’s Respond ventilator, designed for pediatric to adult patients, has received FDA 510(k) clearance as the first U.S.-manufactured ventilator cleared in over 20 years.
Three major manufacturers—Philips Respironics, Baxter Healthcare, and Zoll Medical—have issued Class I recalls for their ventilators due to critical issues posing a risk of serious injury or death.
A state audit finds tens of thousands of ventilators and other devices purchased during COVID-19 remain unused and unmaintained.
Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.
Read MoreBaxter has issued a medical device correction for the Life2000 Ventilation System, citing the potential for patient oxygen desaturation events due to improper use with third-party oxygen concentrators, which may cause patient harm or even death.
Read MoreA team of engineers from MIT are developing a ventilator solution that will aid people with compromised diaphragm function.
Read MorePhilips’ ventilator recall woes, which stemmed from the machines causing patient health issues, are under investigation by French prosecutors.
Read MoreHamilton Medical AG is recalling an intensive care ventilator after complaints revealed a hardware issue with its status indicator board.
Read MoreBreas Medical USA announced the release and immediate availability of the Xpac by Breas extended life battery for ventilators.
Read MoreNew findings may help guide policy makers in deploying ventilators to states with an urgent need of the technology.