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Recalls and Alerts

Class 2 Recall

Class 2 Recall - Dysport 500 Units Powder for Solution for Injection

 

The Medicines and Healthcare products Regulatory Agency (MHRA) has been investigating a report of a falsification of the above product in the UK. The UK Marketing Authorisation Holder has confirmed that the batch above is falsified and has been supplied by unauthorised distributors to the UK.

 

MHRA drug alert date: 22 August 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-dysport-500-units-powder-for-solution-for-injection-el-22-a-slash-36?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=c9c55a5d-d085-47ca-ac0a-6898ac48c6e8&utm_content=immediately

 

 

   Pip code         

          Product Description           

        Supplier          

   Batch Numbers   

 ALLIANCE DO

  NOT STOCK

     Dysport 500 Units Powder

       for Solution for Injection

    Ipsen Limited

        U14534

 

Alliance do not stock the above product so we will not be accepting Customer returns on this recall.

 

Further Information

For medical information enquiries, please contact Ipsen Limited at medinfo.uk-ie@ipsen.com

Recipients of this Medicines Recall should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information.