# The Medicines (Standard Provisions for Licences and Certificates) Amendment Regulations 1977, Paragraph 5


Where the licence holder has been informed by the licensing authority that any batch as aforesaid has been found not to conform as regards strength, quality or purity to the specification of that product or with the provisions of the Act or of any regulations made under the Act that are applicable to the medicinal product, he shall, if so directed and so far as may be reasonably practicable, recall all medicinal products already sold or supplied from that batch.

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Source: https://www.legislation.gov.uk/uksi/1977/675/schedule/5/paragraph/5 (the official version)
Page: https://openlegislation.uk/medicines-standard-provisions-for-licences-and-certificates-amendment-regulations-1977/schedule-5/paragraph-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.