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Recalls and Alerts

Class 4 Caution in Use

Class 4 Caution in use- Co-amoxiclav 125/31.25mg/5ml, 250/62.5mg/5ml powder for oral suspension

Sandoz limited has informed the MHRA that the products mentioned in this notification are not sugar free despite the carton stating ‘sugar free’. The ‘sugar free’ text was added to the carton in December 2008 in error.

MHRA drug alert date: 20th April 2023

 

MHRA drug alert link:  https://www.gov.uk/drug-device-alerts/class-4-medicines-defect-information-sandoz-limited-co-amoxiclav-125-slash-31-dot-25mg-slash-5ml-250-slash-62-dot-5mg-slash-5ml-powder-for-oral-suspension-el-23-a-slash-14?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=8bedc9fd-dd67-44c7-8691-89546eb2ed97&utm_content=immediately#contents

Pip code

Product Description

Livery

Affected Batches

1117290

 

CO-AMOXICLAV 125/31.25MG ALM

 

ALMUS

LL9525 LM7892 MB7218

 

1117308

 

CO-AMOXICLAV 250/62.5MG ALM

 

ALMUS

LM6707 LM7608 MB7828 MG9435

 

1117290

CO-AMOXICLAV 125/31.25MG

SANDOZ

SEE LINK ABOVE

1117308

CO-AMOXICLAV 250/62.5MG

SANDOZ

SEE LINK ABOVE

 

 

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

 

Further Information

For more information, 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