Ambu recalls
All Ambu recalls we track from FDA, CPSC and NHTSA data. Categories: medical devices (11).
11 recalls published between November 6, 2024 and August 20, 2025. Most common issues: mislabeling (1), injury risk (1). 1 was FDA Class I, the most serious level.
- Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult recall
- Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set recall
- KING LTSD,SIZE 2.5, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient… recall
- KING LTSD,SIZE 2, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s… recall
- KING LTSD,SIZE 1, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s… recall
- KING LTSD,SIZE 0, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s… recall
- KING LTSD,SIZE 2.5, W/SUCTION PORT STERILE-Inserted into a patient s… recall
- KING LTSD,SIZE 2,W/SUCTION PORT STERILE-Inserted into a patient s pharynx… recall
- KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx… recall
- AMBU / KING LTSD, SIZE 0,1 W/SUCTION PORT, STERILE- Inserted into a… recall
- Ambu¿ VivaSight 2 DLT Endobronchial tube, 35 FR ( recall