Omnilab Advanced And Bipap A40
Recall Summary Omnilab Advanced and BiPAP A40 devices are being recalled in Canada due to performance issues. The FDA has classified this as a Class I recall, indicating a serious concern. The devices were distributed across Canada.
- Product
- Omnilab Advanced and BiPAP A40
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-08-31
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/313a344e-bcf6-4055-80ab-c211e130339d