Fludeoxyglucose (18F) Injection (FDG)
OFFICIAL-SOURCE RECALL · AUSTRALIA
Fludeoxyglucose (18F) Injection (FDG) Recall: Classification Class II Reason for the Action Batch
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryAustraliaPublishedJuly 24, 2026Last updatedJuly 24, 2026Official source last checkedAugust 26, 2026 at 7:44 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Fludeoxyglucose (18F) Injection (FDG)
- Manufacturer
- See official notice
- Lot number
- numbers, FDG260724A
- Batch number
- numbers, FDG260724A
- Date code
- dates, 24 Jul 2026
- Expiration date
- dates, 24 Jul 2026
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Classification Class II Reason for the Action Batch FDG260724A failed sterility result due to the presence of Lederbergia (Bacillus) sp at 14 days of incubation. Given the nature of the product, this action was undertaken prior to TGA notification (Immediate Market Action as defined within the PRAC). Instructions for Customers/Users Customers are to: - Follow the patient management advice described in the customer letter. Action Commencement Date 24/08/2026 Responsible Entity Queensland Health - Metro North Hospital and Health Service
Hazard
Classification Class II Reason for the Action Batch FDG260724A failed sterility result due to the presence of Lederbergia (Bacillus) sp at 14 days of incubation. Given the nature of the product, this action was undertaken prior to TGA notification (Immediate Market Action as defined within the PRAC). Instructions for Customers/Users Customers are to: - Follow the patient management advice described in the customer letter. Action Commencement Date 24/08/2026 Responsible Entity Queensland Health - Metro North Hospital and Health Service
Official recall notice
Fludeoxyglucose (18F) Injection (FDG)
Agency: Therapeutic Goods Administration
Official publication date: July 24, 2026
Read the official AU_TGA_DRAC recall notice →Scan products you own
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