Monoject Blunt Cannula, Monoject Standard Hypodermic Needles (2019-04-28)

Recall Summary Monoject Blunt Cannula and Monoject Standard Hypodermic Needles have been recalled across Canada due to defects in the medical devices. The recall is classified as Class I, meaning there is a serious potential health risk. This recall affects all Canadian users and distributors of these needle products.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-10

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/baeb0661-d4a9-437b-a7ed-ac72e53ac101