Bivona® Neonatal/pediatric And Adult Tracheostomy Products
Recall Summary Bivona® Neonatal/Pediatric and Adult Tracheostomy Products are being recalled in Canada due to performance issues. This recall applies to tracheostomy tubes used in neonatal, pediatric, and adult patients across the country. The recall is classified as Class I, indicating a serious potential health risk.
- Product
- Bivona® Neonatal/Pediatric and Adult Tracheostomy Products
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-06-03
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/bbb9743d-eda1-461f-89c0-3dc88cc614c7