Ventlab Corporation Issues Nationwide Recall of its Manual Resuscitators

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Ventlab Corporation Issues Nationwide Recall of its Manual Resuscitators

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Ventlab Corporation Issues Nationwide Recall of its Manual Resuscitators

10/19/2012 12:01 PM EDT

On July 11, 2012, Ventlab Corporation initiated a nationwide recall of 14,602 of its manual resuscitators. The manual resuscitators as listed below have been found to potentially deliver little to no air/oxygen through the patient valve to the patient, which could result in life threatening health consequences that include hypoxia and hypoventilation.

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