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Recalls and Alerts

Class 2 Recall

Class 2 recall-Pemetrexed infusion bag 800mg & 1000mg Sun Pharma

Sun Pharmaceutical Industries Europe B.V. is recalling those product batches listed in this notification as a precautionary measure due to out of specification results reported for the Particulate Matter Test (PMT) during stability testing.

 

MHRA drug alert link https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-sun-pharmaceutical-industries-europe-b-dot-v-pemetrexed-1000mg-slash-100ml-10mg-slash-ml-and-800mg-slash-ml-8mg-slash-ml-infusion-bag-el-25-a-slash-09?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=46a9a60c-085d-4255-ad01-adb0b60db794&utm_content=immediately

 

Pip code

Product description

Supplier

Batch Numbers

1264035

PEMETREXED INF BAG 1000MG SUN

SUN PHARMA UK (SUN)

HAF1473A

1263995

PEMETREXED INF BAG 800MG SUN

SUN PHARMA UK (SUN)

HAF0544A

 

Further Information

For stock control enquiries please contact Customer Service UK Cserv.uk@sunpharma.com or phone (0) 20 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.