Nucletron B.v. Intrauterine Tube

Nucletron B.V. is recalling their Intrauterine Tube due to a device performance issue. The recall affects units distributed across Canada. This is classified as a Class II recall, which indicates a potential health risk but not an immediately life-threatening situation.

Product

Nucletron B.V. Intrauterine Tube

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-04-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4c010305-b369-44cd-a175-ba446e4f93f2