Emerade Injection; Device Failure

Emerade Injection (0.3 mg/0.3 mL and 0.5 mg/0.5 mL) is being recalled across Canada because the device may fail to work properly. This is a Class I recall, meaning there is a serious risk to health. The recall affects all Emerade injections distributed in Canada.

Product
Emerade Injection (0.3 mg / 0.3 mL and 0.5 mg / 0.5 mL)
Reason
Product quality
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2023-05-08
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/7686bbf0-dee0-4e25-b1ef-3200cf2fb370