Remifentanil Hydrochloride For Injection; Out Of Specification (assay & Impurity)

Remifentanil hydrochloride for injection 1 mg/vial is being recalled across Canada because testing found the product did not meet required quality standards for drug purity and active ingredient content. This is a Class II recall, meaning the product could cause temporary or medically reversible health effects. The recall affects remifentanil hydrochloride injectable medication distributed nationwide in Canada.

Product
Remifentanil hydrochloride for injection 1 mg/vial
Reason
Product quality concern
Classification
Class II
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2026-06-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/6a784a66-ad11-4308-942e-f94dc6945173