The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
The ongoing surge in positive COVID-19 cases has caused a significant equipment shortage, resulting in health systems needing to borrow medical devices.Read More
The U.S. FDA has revealed that Medtronic’s recall of certain Puritan Bennett ventilators is Class 1—which means that using the devices could result in serious patient harm or even death.Read More
Lithium ion batteries are widely used in life-saving medical devices critical to everyday patient care and the fight against COVID-19.Read More
The COVID-19 pandemic caused an immeasurable number of delays to the healthcare supply chain, which included a large bulk order of ventilators in Iowa.Read More
Philips is scrutinizing a recall of its ventilators and respiratory devices from the U.S. FDA.Read More
The U.S. FDA is providing an update related to the June 14, 2021, recall of certain Philips Respironics ventilators, continuous positive airway pressure (CPAP), and bilevel positive airway pressure (BiPAP) machines.Read More