Product description
Batch No. 87255 - 60mL bottle. No other batches of Combantrin Suspension or other Combantrin products are affected.
See a list of details to help identify the product
Reason the product is recalled
The contents of this specific batch do not mix effectively when following the pack instructions (shaking the bottle well for approximately 20 seconds). This can give rise to dosing error in the use of the product.
The hazards to consumers
Illness or mistreatment (Class II).
What consumers should do
If you have a bottle of Combantrin Suspension from batch 87255 do not use it. Return the product for a full refund to either the place of purchase, to Johnson & Johnson Pacific Pty Limited, Combantrin, Reply Paid 74903, Locked Bag 5 Broadway NSW 2007 Australia or telephone the Consumer Service Centre on 1800 733 821 for instructions to return the product.
Details to help identify the product
Supplier running the recall
Johnson & Johnson Pacific Pty Limited
Identifying product features
The batch number is located on the top of the product pack as well as on the back of the Combantrin bottle label. ARTG No. 10747
Identifying numbers
Other identifying numbers
The batch number is located on the top of the product pack as well as on the back of the Combantrin bottle label. ARTG No. 10747
Where the product was sold
Nationally
Responsible regulators
Regulators are established or appointed by government. They enforce regulations and rules.
Quote PRA number 2007/9317 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.