The Department of Health today (September 12) instructed Advance Pharmaceutical Co Limited, a licensed drug manufacturer, to recall one batch (Batch No: 35262) of its product Duoflue Cold Tablet 1000's (Registration No: HK-37595) from the market because the new revised label shows a wrong quantity of 500mg for the ingredient paracetamol. The correct quantity should be 150mg of paracetamol.   Close