Complications Associated with AMBU™ Scope Use: An FDA MAUDE Analysis

Ambu® aScope™ is a disposable flexible videoscope used for a wide range of medical procedures. However, adverse events associated with this device can occur. The Food and Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database was explored for patient‐related adverse events associated with Ambu® aScope™ use between January 1, 2000 and December 15, 2023. Search terms included “Ambu” and “Ascope.” Thirty unique adverse events were identified. Twenty‐one of the events were associated with patient injury, and 9 with device malfunction. Eight patient‐reported problems were documented as foreign bodies, 3 events as airway obstruction, desaturation, or hypoxic events, and 1 event as anxiety/cardiac arrest. The remaining 18 reported insufficient information other than associated with patient injury. We found that Ambu® aScope™ flexible nasolaryngoscopes and bronchoscopes are a common and effective tool for airway evaluations that may infrequently serve as a rare form of foreign body with potentially life‐threatening consequences.