Brand

Ambu Inc. Recalls

6 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Ambu Inc..

6Total Recalls
3Critical
162,425Units Affected
Jul 9, 2025Most Recent
All Recalls

Every Ambu Inc. Recall

Sorted by most recent. Click any recall for full details.

6 recalls
CriticalFDA
Ambu Inc.
Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Merc...
Medical Devices·87,156 affected·Jul 9, 2025
High RiskFDA
Ambu Inc.
Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR (Catalog Number 412351000), 37 Fr (Catalog Number 412371000), 39 Fr (Catalog Number 41239...
Medical Devices·1,824 affected·Sep 16, 2024
CriticalFDA
Ambu Inc.
Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
Medical Devices·11,845 affected·Dec 5, 2023
CriticalFDA
Ambu Inc.
Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, port...
Medical Devices·2,689 affected·Jul 21, 2023
High RiskFDA
Ambu Inc.
Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 4123710...
Medical Devices·12,921 affected·Jun 3, 2022
High RiskFDA
Ambu Inc.
Ambu, Aura Gain - Single Use Laryngeal Mask- Sterile for use as an alternative to a face mask for achieving and maintaining control of ...
Medical Devices·45,990 affected·Feb 10, 2016