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Recalls and Alerts

Class 4 Caution in Use

Class 4 caution in use-Risperidone 1mg, 2mg & 3mg tablets

Sandoz Ltd. has informed the MHRA that there is missing safety information in the Patient Information Leaflet (PIL) and Summary of Product Characteristics (SmPC) for Risperidone 1mg, 2mg and 3mg and Tablets.

 

MHRA Drug alert date: 26th September 2024

 

MHRA drug alert link:https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-sandoz-ltd-dot-risperidone-1mg-2mg-3mg-tablets-el-24-a-slash-43?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=b4d60715-056e-4313-977a-7a57a225af0e&utm_content=immediately

 

Pip code

Product description

Supplier

Batch Numbers

1159102

RISPERIDONE TAB 1MG (20)

SANDOZ LTD

NK4910

1159110

RISPERIDONE TAB 1MG (60)

SANDOZ LTD

NK4909

1159128

RISPERIDONE TAB 2MG (60)

SANDOZ LTD

NL4679

1159136

RISPERIDONE TAB 3MG (60)

SANDOZ LTD

MM5115  NE5508

 

 

This is a caution in use only we are not accepting stock returns

 

Further Information

For medical information queries, please contact: sandozgb@EU.propharmagroup.com, Telephone: +44 1276 698 101.

 

For stock control queries, please contact: sales.sandoz-gb@sandoz.com, Telephone: +44 1276 698607.