After more than 18 months of discussions, Royal Philips announced on 29 January that it has agreed with the US Department of Justice (DoJ) and Food and Drug Administration (FDA) the terms of the consent decree detailing how the company must change its manufacturing in the wake of the Respironics, Inc. product recalls.
Two US recall notices in June 2021 centering around breathing technologies within the sleep and respiratory care (S&RC) portfolio were the start of what turned into an ongoing crisis management exercise for one of the world’s top ten medtech companies by revenues (2022 data)