Products
AirBoss Defense Group recently notified customers that certain FlexAir Powered Air Purifying Respirators supplied to the Federal Emergency Management Agency to facilitate COVID-19 pandemic response must be replaced or retrofitted for continued National Institute for Occupational Safety and Health…
Philips Respironics is recalling all V60 and V60 Plus ventilators due to an internal power fluctuation error.
Atrium Medical Corporation has recalled the iCast Covered Stent System.
The Food and Drug Administration approved the first generic version of Symbicort, a metered-dose inhaler for asthma and chronic obstructive pulmonary disease.
Fresenius Kabi USA recalledseven lots of sodium acetate injection after finding particulate matter in sample vials, which could cause infection or other serious adverse events if administered. No adverse events were reported.
B. Braun Medical Inc. has recalled five lots of 0.9% sodium chloride for injection due to fluid leakage or low fill volume, which could pose an infection risk to patients, the Food and Drug Administration announced.
Ellume has expanded its recall of rapid at-home COVID-19 antigen tests to about 2 million tests, the Food and Drug Administration said in an update this week.
Health care providers should not purchase or use certain imported medical gloves from certain companies, which appear to have been reprocessed, cleaned or recycled and sold as new, the Food and Drug Administration announced.
The Food and Drug Administration announced a Class 1 recall of battery packs for an intra-aortic balloon pump used with patients undergoing surgery and to treat adults with acute coronary syndrome or heart failure complications.
The Food and Drug Administration approved the first interchangeable biosimilar product for Humira, a monoclonal antibody used to treat certain inflammatory diseases.