OFFICIAL-SOURCE RECALL · AUSTRALIA
Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) Recall: 25/09/2026 Cefazolin 6,000mg in 0
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) for Intravenous Infusion
- Manufacturer
- See official notice
- Lot number
- BB260819555
- Batch number
- BB260819555
- Date code
- 23/11/2026 ARTG Exempt ARTG Num
- Expiration date
- 23/11/2026 ARTG Exempt ARTG Num
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
25/09/2026 Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) for Intravenous Infusion Medicine Recall Class II Hospital
Hazard
25/09/2026 Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) for Intravenous Infusion Medicine Recall Class II Hospital
Official recall notice
Cefazolin 6,000mg in 0.9% Sodium Chloride in Surefuser + (10mL/hr) for Intravenous Infusion
Agency: Therapeutic Goods Administration
Official publication date: September 25, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
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