The FDA has received reports of airway obstruction and ventilation failure for certain EMG endotracheal tubes. Link to original article Baxter Healthcare Corporation Recalls Clearlink Basic Solution Set with Duovent for Risk of Leaks That May Expose Providers and Patients to Hazardous / Toxic Substances Recommendations for Certain Medtronic Electromyogram Endotracheal Tubes and Risk of Airway Obstruction – Letter to Health Care Providers Share Print Please login or register to post comments.