|
 
Mercury Medical is recalling Neo-Tee Resuscitators due to the potential for the inline controller to come apart, causing a loss of positive pressure that will impact effective ventilation of the patient and prevent the inline controller from being used.
The U.S. Food and Drug Administration (FDA) has identified this as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it.
Questions?
Customers in the U.S. with questions about this recall should contact their Mercury Medical sales representative or the Mercury Medical team at 800-237-6418/727-573-0088 or regulatoryaffairs@mercurymed.com.
|
|
|
|