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Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines.

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Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines.

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Some Philips Respironics DreamStation Devices Recalled

There are 1,088 devices recalled in the U.S., the FDA said

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FDA: Some Philips CPAP, BiPAP machines may not work as intended

The U.S. FDA issued a Class I recall, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines.

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FDA Roundup: April 7, 2023

FDA Roundup: April 7, 2023
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