Wyeth Australia Pty Ltd—Phospholine iodide (echothiophate iodide for ophthalmic solution)

Identifying features

N/A

What are the defects?

Eyedroppers were not subject to sterilization, which could cause a lack of assurance of sterility.

What are the hazards?

Illness or mistreatment (Class II).

What should consumers do?

N/A

Supplier
Wyeth Australia Pty Limited
Where the product was sold
Nationally

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category