Product description
6.25mg/5mL (0.125%). Lots Nos. 1076-55 (exp 04/08), 1076-57 (Exp 11/08).
See a list of details to help identify the product
Reason 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
Details to help identify the product
Supplier running the recall
Wyeth Australia Pty Limited
Identifying product features
N/A
Identifying numbers
Other identifying numbers
N/A
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2007/9661 when contacting a regulator about this recall.
Recall and remedy questions
Contact the Therapeutic Goods Administration if you have:
- a question about the remedy being offered to you by the business that is responsible for managing this recall, or
- concerns about the way the business is managing this recall.