Class 3 recall- Fingolimod SUN 0.5mg hard capsules

CLASS 3 RECALL

Class 3 Recall from Sun Pharmaceutical Industries Limited

on Fingolimod SUN 0.5mg hard capsules

MHRA drug alert link https://www.gov.uk/drug-device-alerts/class-3-medicines-recall-sun-pharmaceutical-industries-limited-fingolimod-sun-0-dot-5mg-hard-capsules-el-25-a-slash-49?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=43ceb057-770e-45c5-b999-ad92df38ac1a&utm_content=immediately

MHRA ref: PL 31750/017

Reason: “Sun Pharma UK Limited is conducting a precautionary recall of a single batch of Fingolimod SUN 0.5 mg hard capsules due to reports of capsule breakage on removing from the blister. No other batches of Fingolimod SUN 0.5mg hard capsules are impacted.”

Please can you ensure that your stores quarantine the product listed below.

Further Information

For all medical information enquiries and information on this product, please email Cserv.uk@sunpharma.com, or telephone 020 8848 5050 / 07974754551.

For stock control enquiries please email Cserv.uk@sunpharma.com, or telephone 020 8848 5050.

Please return all affected stock to your original supplier for credit. Unfortunately, we can only accept stock purchased from us (Alliance Healthcare Distribution Limited). Any other stock will be returned to your stores/Pharmacies.

Please note that anything not returned to us, or notified to us, within 3 months of this notification, cannot be reimbursed by way of a credit.