Ambu recalls

Ambu appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2025-08-20.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercur…
  FDA Device · Class I · 2025-08-20 · Ambu
• Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set
  FDA Device · Class II · 2025-05-14 · Ambu
• Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 4123910…
  FDA Device · Class II · 2024-11-06 · Ambu
• Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
  FDA Device · Class II · 2024-01-17 · Ambu
• Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portab…
  FDA Device · Class II · 2023-10-04 · Ambu
• Ambu VivaSight 2 DLT
  FDA Device · Class II · 2022-07-27 · Ambu
• Ambu, Aura Gain - Single Use Laryngeal Mask- Sterile for use as an alternative to a face mask for achieving and maintaining control of the…
  FDA Device · Class II · 2016-03-30 · Ambu