Recall stamp

O-Two Medical Technologies Recalls Transport Ventilators

April 8, 2019

The FDA identified O-Two Medical Technologies’ recall of its automatic transport ventilator devices as a Class I recall.

The recalled devices, the e500, e600 and e700 automatic transport ventilators, are used while a patient travels to or between hospitals and in transport settings. It was found that the devices posed risks of fires due to improper screw placement in their screens.

The devices are used for adults, children and infants that are in cardiac arrest or respiratory distress and need help breathing.

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