Dlp Vessel Cannulae

DLP Vessel Cannulae Recall Summary DLP Vessel Cannulae are being recalled across Canada due to labelling and packaging issues. This is a Class I recall, which is the most serious classification. The affected product is distributed nationwide in Canada.

Product
DLP Vessel Cannulae
Reason
Labelling and packaging
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-02-22
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/904b3344-c653-4520-a22f-53cf7fb95d57