Johnson & Johnson Pacific Pty Limited—Combantrin Suspension 50mg/mL

PRA number

2007/9317

Published date

Product description

Batch No. 87255 - 60mL bottle. No other batches of Combantrin Suspension or other Combantrin products are affected.
Identifying 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

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

Reasons 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.

Supplier

Johnson & Johnson Pacific Pty Limited

Where the product was sold

Nationally

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category

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