Eligard 7.5mg: May Not Be Filled With Correct Amount Of Leuprolide Acetate.

ELIGARD 7.5mg injectable vials distributed in Canada may contain an incorrect amount of the active ingredient leuprolide acetate. This is a Class I recall, meaning there is a potential serious adverse health consequence. The affected product was distributed across Canada.

Product
ELIGARD 7.5mg
Reason
Product quality
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2023-09-12
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/cdb5224c-d383-4f80-b3e1-194b378681d7