In the interest of public health it may be necessary to withdraw a batch of medicinal products from the market as soon as possible. All authorised manufacturers are obliged to make an effective a system for withdrawing activities. The Marketing Authorisation Holder is obliged to notify the competent authority about all defects or other factors which may result in the withdrawal of a medicine from the market.
The list of withdrawals and suspensions available only in Hungarian: https://ogyei.gov.hu/kivonas_felfuggesztes/
