Guider Softtip Xf (2017-12-13)

Guider SoftTip XF Recall Summary Guider SoftTip XF medical devices are being recalled across Canada due to a safety issue. This recall affects all units of this product that were distributed in Canada. The recall is classified as Class I, indicating a serious potential health risk associated with the device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-01-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/7448429f-cbdb-42ec-b038-591672ea0e44