| Subject: | Recall of Single-Patient Use Manual Pulmonary Resuscitator |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 7 Oct 2009 - 03:00 pm |
| The Food and Drug Administration (FDA) and Unomedical have notified healthcare professionals about the recall of the single-patient use Manual Pulmonary Resuscitator because of a malfunction that may impair the ability of the device to generate the positive pressure necessary to function properly which could potentially cause serious adverse health consequences or death. The recalled resuscitators were manufactured from July 2002 through March 2008. Please see Unomedical's... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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