Support Alert

Company led recall: Furosemide-Claris 20mg/2ml Injection

11 Aug 2016

The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a company-led recall for Furosemide-Claris 20mg/2ml Injection (Marketing Authorisation number AUST R 148003) manufactured by Claris Lifesciences UK Ltd. Pharmacists and wholesalers are asked to check packs as they have been inadvertently distributed in the UK and are intended for the Australian market.

Further details of the alert and the affected batch are available on the MHRA website.

 
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