Product recalls and crucial regulatory compliance procedures are the main barriers to the growth of the North American respiratory trainer market. For instance, the U.S. Food and Drug Administration (FDA) ordered Philips Respironics, a manufacturer of medical devices, to recall millions of sleep and respiratory devices in July 2021 due to concerns that foam used in the devices to reduce sound and vibration could crack and enter the air hose of the device, where it could be inhaled by the user.
As a result, the Military Health System (MHS) informed all TRICARE-authorized DME providers of the recall. MHS also requested that prescribing physicians assist in informing patients of the recall and establish whether they were given a medical device on the Philips recall list.
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https://knackersblogger.blogspot.com/2022/09/north-america-respiratory-trainer.html
Click here for North America Respiratory Trainer Market Press Release:
https://www.coherentmarketinsights.com/press-release/north-america-respiratory-trainer-market-4178
