Tag: respiratory equipment

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Trudell Medical Limited is set to acquire the RDx business unit from Vyaire Medical, expanding its market in respiratory diagnostics.

Alveofit announces that its respiratory device, Alveoair spirometer, has earned FDA clearance for distribution in the United States.

Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.

Trudell Medical Limited is set to acquire the RDx business unit from Vyaire Medical, expanding its market in respiratory diagnostics.

Oct 25, 2022

Medtronic intends to pursue a separation of the company’s combined patient monitoring and respiratory Interventions businesses.

Sep 28, 2022

Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.

Sep 23, 2022

Philips RS has agreed to pay nearly $1.3 million to settle allegations that it violated the False Claims Act and Anti-Kickback Statute.

Sep 7, 2022

Philips has recalled certain masks used with bilevel positive airway pressure machines and CPAP machines due to a serious safety concern.

Sep 2, 2022

Philips RS North America a manufacturer of durable medical equipment agreed to pay over $24 million to resolve False Claims Act allegations.

Aug 30, 2022

Philips recalled certain bi-level positive airway pressure machines that may contain a plastic contaminated with a non-compatible material.

The U.S. FDA announced the removal of N95 respirators from its medical device shortage list, signaling that demand no longer exceeds supply.