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.
FDA MedWatch Safety Alert. Unomedical Manual Pulmonary Resuscitator – Recall. October 7, 2009.