Lina Librata-endometrial Ablation Device (2017-10-06)

LiNA Librata Recall Summary The LiNA Librata endometrial ablation device is being recalled across Canada because of a manufacturing defect that may affect how the device functions during the procedure. This device is used to treat abnormal uterine bleeding by ablating (removing) the tissue lining the uterus. The recall affects all units of this device that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-10-20

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f3990f4e-a8b7-4108-af5e-a1e7135e9bc7