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).
Reasons the product is recalled
Eyedroppers were not subject to sterilization, which could cause a lack of assurance of sterility.
The hazards to consumers
Illness or mistreatment (Class II).
What consumers should 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.