New Taipei City, N/A, Taiwan
Besmed Health Business Corporation recalls
1 recall recorded since 2018, most recently on 9 August 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 9 August 2018
- Terminated
- 10 May 2019
- Reason
- Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask Sterile
- Distribution
- US Nationwide, and country of Canada.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0109-2019
- Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.