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Jul 27, 2022newest stored source record
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Medical DeviceJul 27, 2022

Ambu VivaSight 2 DLT recall — FDA Z-1420-2022

Firm has received complaints on the device concerning leak/rupture of either the bronchial or tracheal cuff. Leakage during procedure could lead to loss of secure airway and will require…

Class IIFDA: OngoingAmbu Inc.
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