Ambu Inc.
6 recalls on record · Latest: Aug 20, 2025
FDA Devices Critical Aug 20, 2025
Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, …
FDA Devices Moderate Nov 6, 2024
Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 412391000), 41 Fr…
FDA Devices Moderate Jan 17, 2024
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
FDA Devices Moderate Oct 4, 2023
Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portable endosco…
FDA Devices Moderate Jul 27, 2022
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000, 412391…
FDA Devices Moderate Mar 30, 2016