Wyeth Australia Pty Ltd—Phospholine iodide (echothiophate iodide for ophthalmic solution)
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?
Wyeth Australia Pty Limited
Where the product was sold
Therapeutic Goods Administration is the responsible regulator for this recall.