B12lt Reprocessed Endoscopic Bladeless Trocar (2017-12-04)

Recall Summary Reprocessed B12LT endoscopic bladeless trocars (surgical instruments used in minimally invasive procedures) are being recalled across Canada because they do not meet sterility and safety standards required for reuse. The recall affects all units of this reprocessed device distributed in Canada. This is classified as a Class I recall, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/69f2e601-0e9d-4771-9880-7b8ebeaa8495