Fludeoxyglucose (18F) Injection; Cracket vial

Product Fludeoxyglucose (18F) Injection Issue Health products - Product quality What to do Consult your health care professional if you have any health concerns. Audience Healthcare

Fludeoxyglucose (18F) vial containing 24.80 mL (30.23 GBq of the product) used to administered the drug to the patients was found to be broken at the bottom.

Verify if your product is affected. Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns. Contact the recalling firm if you have any questions about the recall. Report any health product related side effects to Health Canada. Report any other health product safety complaints to Health Canada.

RA-82272