Synchro 2/ Guidewire (soft, Standard) (2019-03-04)

Recall Summary Synchro 2 and Guidewire devices (both Soft and Standard versions) are being recalled across Canada due to a medical device issue. This recall affects all units distributed in Canada since the product's introduction.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-03-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a795d93c-018c-420e-87fd-7f50eedb07b8