AstraZeneca Pty Ltd—Heparinised saline 50IU/5ml, packs of 50 ampoules

Identifying features

ARTG number 12107

What are the defects?

The detection of a contaminant in the Heparin raw material used to manufacture these batches.

What are the hazards?

Illness or mistreatment (Class II).

What should consumers do?


AstraZeneca Pty Ltd
Where the product was sold

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category