14,602 manual resuscitators have been recalled by the Ventlab Corporation. These resuscitators, which were available between March and July of this year, might not deliver the requisite amount of air to a patient in need of the device. Hypoventilation and hypoxia could then become a distinct possibility, and the issue could even be lethal. Thankfully, no one has reported any type of injury at this point in time, and the company that initiated the recall is in the process of providing users with a remedy.
Follow this link for more about the recall.