Lina Librata, Endometrial Ablation Device
Lina Librata Endometrial Ablation Device Recall The Lina Librata endometrial ablation device is being recalled in Canada due to issues with its labelling and packaging. This is a Class I recall, which indicates a serious issue. The device was distributed across Canada.
- Product
- Lina Librata, Endometrial Ablation Device
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-02-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/44a564d7-26cc-4bcd-b18e-646066921de1