Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

Here are four of the latest recalls and corrections reported to the FDA.

Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.

The number of cases saw a 50% increase over last year, but Health Commissioner Dr. Amler said the information "was not a cause for undue alarm." ...

Portable power stations are incredibly popular, but it can be hard to distinguish between quality models and cheap mass-produced ones. […] The post Nebo Intrepid 1000 Power Station: Reliable, Stable ...

With the number of local Legionnaires’ disease cases up to 34 as of Tuesday afternoon, State Epidemiologist Dr. Matthew ...

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