Swan-ganz Double Lumen Monitoring Catheter
Swan-Ganz Double Lumen Monitoring Catheter Recall Edwards Lifesciences is recalling Swan-Ganz Double Lumen Monitoring Catheters across Canada due to labelling and packaging issues. This is a Class I recall, meaning the product could cause serious harm or death. The catheters were distributed nationwide in Canada.
- Product
- Swan-Ganz Double Lumen Monitoring Catheter
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-07-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/0feefc48-a8a4-4f26-bb4c-4e0518b333b3