Class 3 medicines recall: Theramex Ireland Ltd T/A Theramex HQ UK Ltd, AlfaD capsules

Theramex Ireland Ltd T/A Theramex HQ UK Ltd has informed the Medicines and Healthcare products Regulatory Agency (MHRA) of an issue related to an error in the decommissioning of two batches of AlfaD capsules. Upon decommissioning at the pharmacy and when scanning the serialised 2D code, the status of packs may report as ‘EXPORT’. Although there is no risk to product quality, any remaining stock should be quarantined and returned.

Further information including details of the affected batches and advice for healthcare professionals can be found on the MHRA website.