Reprocessed Ethicon Xcel Bladeless Trocar (h12lp)

Recall Summary Ethicon XCEL Bladeless Trocar (H12LP) devices that have been reprocessed are being recalled across Canada due to concerns that the reprocessing may have compromised the device's safety and effectiveness. These trocars are surgical instruments used during minimally invasive procedures to create access points in the body. The recall affects healthcare facilities and surgical centers in Canada that have received these reprocessed devices.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-11-25

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4d0a3c5f-7a41-4d82-bb08-a23e882f22a4