FDA recalls 2 ventilator models

12/27/2012 | MedPage Today (free registration)

The FDA has recalled two ventilator-related devices. The Ventlab manual resuscitator was found to have a potentially leaking valve that could result in little or no airflow to the patient. The Bunnell Life Pulse High-Frequency Ventilator Patient Circuit, used for critically ill infants, has heater wire insulation that can melt, causing sparking and smoke.

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