viernes, 10 de agosto de 2018

FDA MedWatch Recall Notice - AirLife Resuscitation Devices by: Vyaire Medical - Recalled Due to Manufacturing Error Preventing Oxygen Delivery

U.S. Food and Drug Administration Header

A new MedWatch Safety Alert recall: AirLife Resuscitation Devices by: Vyaire Medical - Recalled Due to Manufacturing Error Preventing Oxygen Delivery was just added to the FDA Recalls webpage.
 

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