Portex Blue Line Ultra Tracheostomy Tube Inner Cannula (2019-02-10)
Portex Blue Line Ultra Tracheostomy Tube Inner Cannula Recall Portex Blue Line Ultra tracheostomy tube inner cannulas are being recalled in Canada because they may not function properly. The inner cannulas, which are medical devices used in tracheostomies, were distributed across Canada. This is a Class I recall, meaning the product could cause serious harm or death.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-02-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e4d99906-a30e-4daa-bc91-079c2a93760e