Medtronic’s HVAD system recalled again amid driveline cover problems

New issues have continued to surface with the problem-plagued device even after Medtronic pulled it from the market last year.

By Elise Reuter • Dec. 1, 2022

Philips respirator recall reaches 260 reported deaths, FDA says

The agency has received 90,000 medical device reports related to foam problems with Philips’ recalled sleep apnea devices and ventilators.

By Elise Reuter • Updated Nov. 23, 2022

Philips’ ventilator woes grow as FDA issues alert over replacement foam

Replacement noise reduction material in Trilogy ventilators can block the air inlet and let trace amounts of particulate matter into the air pathway.

By Nick Paul Taylor • Nov. 18, 2022