Philips Respironics has issued a software correction to address previously reported safety concerns for its Trilogy ventilators, which provide breathing support to patients in various settings.
Latest Philips Recall Linked To Death, Injuries
Philips has issued a recall of various Trilogy ventilators due to safety issues that may affect their ability to properly function. The US FDA has designated the recall class I, its most serious.

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Pediatric devices and IVDs are to be a priority. And the European Health Data Space regulation is seen as critical in supporting digital technologies and AI in transforming care.