Ambu Inc.
Columbia, MD
This page shows every FDA and USDA recall linked to Ambu Inc.. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
7
Total Recalls
2016
First Recall
2025
Most Recent
Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR I...
Aug 13, 2025
· Device
Open, Classified
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
May 6, 2025
· Device
Open, Classified
Ambu VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 3...
Oct 30, 2024
· Device
Open, Classified
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Jan 11, 2024
· Device
Open, Classified
Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu...
Sep 22, 2023
· Device
Open, Classified
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog n...
Jun 3, 2022
· Device
Open, Classified
Ambu, Aura Gain - Single Use Laryngeal Mask- Sterile
for use as an alternative to a face mask for achieving a...
Mar 24, 2016
· Device
Terminated