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Medicine recall – Valsartan; Actavis and Dexcel brands

July 6, 2018

Please be aware that pharmacy has been notified of a class 1 (immediate action) recall on Valsartan branded products (Actavis and Dexcel tablets and capsules). The recall is due to possible chemical contamination.

The affected products are:

Product name marketing authorisation holder PL number
Valsartan 40mg capsules, hard Dexcel pharma limited PL 14017/0192
Valsartan 80mg capsules, hard Dexcel pharma limited PL 14017/0193
Valsartan 160mg capsules, hard Dexcel pharma limited PL 14017/0194
Valsartan 40mg film-coated tablets Actavis group ptc ehf PL 30306/0109
Valsartan 80mg film-coated tablets Actavis group ptc ehf PL 30306/0110
Valsartan 160mg film-coated tablets Actavis group ptc ehf PL 30306/0111
Valsartan 320mg film-coated tablets Actavis group ptc ehf PL 30306/0405

 

Pharmacy can confirm it does not have the affected products.

Please be aware, patients may present to us with the affected products and we may be using their supply of affected products on wards (patient’s own drugs). All nursing and medical colleagues are urged to check with patients who either are prescribed Valsartan, or who have Valsartan on the drug histories (which can be seen as the green drug history form in the patient’s case notes) if they have the affected products.

If affected products are found, please remove them immediately and quarantine them. Inform pharmacy immediately (out of hours through the on-call pharmacist) and we will remove the products and organise a supply of unaffected product (the following day if out of hours).

For further information, please visit gov.uk or contact Medicines Information on ext. 5259.