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Recall of five valsartan-containing pharmaceutical products (with photos)
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     The Department of Health (DH) today (July 6) instructed two licensed medicine wholesalers, namely Actavis Hong Kong Limited and Hong Kong Medical Supplies Ltd (HK Medical), to recall five products containing valsartan from the market as a precautionary measure due to an impurity detected in the raw material.
 
     The affected products are:
 
Product Hong Kong Registration Number Registration certificate holder
Valtensin 160mg tablets HK-61786 Actavis
Valtensin 80mg tablets HK-61787 Actavis
Valtensin HCT tablets 160/12.5mg HK-61784 Actavis
Valtensin HCT tablets 80/12.5mg HK-61785 Actavis
Valsartan Stada 80mg tablets HK-60794 HK Medical
 
     The DH, through its surveillance system, noted that the raw material valsartan produced by a manufacturer in the Mainland and used in certain pharmaceutical products as an active ingredient was found to contain an impurity, N-nitrosodimethylamine (NDMA). NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests.
 
     So far, the above products registered in Hong Kong are confirmed by the wholesalers to contain the affected raw material. The DH's investigation is continuing.
 
     According to the preliminary investigation of the Mainland manufacturer, the presence of NDMA in the raw material valsartan is believed to be related to its production method.
 
     Valsartan-containing products are prescription medicines used to treat hypertension and heart failure. They are available as single ingredient products or in combination with other active ingredients.
 
     According to Actavis and HK Medical, the above products have been supplied to local private doctors and pharmacies. The products Valtensin 80mg and 160mg tablets have also been supplied to the Hospital Authority.
 
     Both companies have set up hotlines (Actavis: 3188 4288; HK Medical: 2806 3112) to answer related enquiries.
 
     So far, the DH has not received any adverse reactions related to the above affected products.
 
     Patients who are taking the above products should not stop taking the medicines, but should seek advice from their healthcare professionals for appropriate arrangement.
 
Ends/Friday, July 6, 2018
Issued at HKT 20:26
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The Department of Health today (July 6) instructed two licensed medicine wholesalers to recall five products containing valsartan from the market. Picture shows two of the affected products, namely Valtensin 160mg tablets and Valtensin 80mg tablets.
The Department of Health today (July 6) instructed two licensed medicine wholesalers to recall five products containing valsartan from the market. Picture shows two of the affected products, namely Valtensin HCT tablets 160/12.5mg and Valtensin HCT tablets 80/12.5mg.
The Department of Health today (July 6) instructed two licensed medicine wholesalers to recall five products containing valsartan from the market. Picture shows one of the affected products, Valsartan Stada 80mg tablets.