Fludeoxyglucose (18f) Injection: Sterility Testing Could Not Be Performed For The Affected Lot

Recall Summary Fludeoxyglucose (18F) Injection from an affected lot was recalled because sterility testing could not be completed to confirm the product was free from contamination. This is a Class I recall, meaning there is a reasonable possibility that use of the product could cause serious adverse health consequences or death. The affected product was distributed across Canada.

Product
FLUDEOXYGLUCOSE (18F) INJECTION
Reason
Product quality
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DRUGS
Recall date
2023-11-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DRUGS

Recall details on Nibble Recalls: https://trynibble.app/recalls/6804f710-6f93-46c8-a178-17732837cd68