Health product recall

FLUDEOXYGLUCOSE (18F) INJECTION: Sterility testing could not be performed for the affected lot

Last updated

Summary

Product
FLUDEOXYGLUCOSE (18F) INJECTION
Issue
Health products - Product quality
What to do

Consult your health care professional if you have any health concerns.

Affected products

Brand Product Name Market Authorization Dosage Form Strength Lot
FLUDEOXYGLUCOSE (18F) INJECTION FLUDEOXYGLUCOSE (18F) INJECTION DIN 02412837 Solution 18F Fludeoxyglucose (18F-FDG) 71.8 GBq G20231011

Issue

Sterility testing could not be performed for the affected lot.

What you should do

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

Additional information

Background

Depth of recall: Healthcare establishments

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies

Winnipeg Regional Health Authority

SR061-820 Sherbrook Street, Winnipeg

MB R3A 1R9

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type III
Identification number
RA-74517