Unomedical Manual Pulmonary Resuscitator - Recall
MedSun: Newsletter #42, November 2009

FDA MedWatch Safety Alert

Unomedical and FDA notified healthcare professionals about the recall of the single-patient use Manual Pulmonary Resuscitator because of a malfunction which may impair the ability of the device to generate the positive pressure necessary to function properly and could potentially cause serious adverse health consequences or death.

Additional Information:

FDA MedWatch Safety Alert. Unomedical Manual Pulmonary Resuscitator – Recall. October 7, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm185702.htm


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