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

PRA number

2007/9661

Published date

Product description

6.25mg/5mL (0.125%). Lots Nos. 1076-55 (exp 04/08), 1076-57 (Exp 11/08).
Identifying features
N/A

Other identifying numbers

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

Pharmacy