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Recalls and Alerts

Class 4 Caution in Use

Class 4 Caution in use- Lemsip Max cold and flu capsules

Reckitt Benckiser Healthcare (UK) Limited has informed the MHRA that a typographical error has been identified on the end flap of the outer carton of some batches of Lemsip Max Cold & Flu Capsules.

 

MHRA drug alert date: 23rd February 2023

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-reckitt-benckiser-healthcare-uk-limited-lemsip-max-cold-and-flu-capsules-el-23-a-slash-04?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=c26db05c-8d64-472f-a107-53c53ded316e&utm_content=immediately

 

Pip code

Product

Supplier

Affected Batches

2531101

LEMSIP MAX COLD AND FLU CAPSULES (16)

RECKITT BENCKISER   

AED954
AED955
AED956
AED957
AED958
AED960
AED961

2531119

 

LEMSIP MAX COLD AND FLU CAPSULES (8)  

RECKITT BENCKISER   

AED981
AEE003

 

 

 

 

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

 

Further Information

For medical information and stock control queries please contact: ConsumerHealth_GB@Reckitt.com and / or 03332005345.