ATTENTION: Please enable Javascript in your browser for full site functionality.
Skip to navigation Skip to main content Skip to footer

Recalls and Alerts

Class 2 Recall

CLASS 2 RECALL - STEMETIL 5MG/5ML SYRUP

 

Sanofi is recalling all batches of the above product as a precautionary measure due to the identification of N-nitrosomethylphenylamine (NMPA) above the acceptable limit. Nitrosamines may increase the risk of cancer if people are exposed to them above acceptable levels and over long periods of time.

 

MHRA drug alert date: 10 October 2022

 

MHRA drug alert link: https://www.gov.uk/drug-device-alerts/class-2-medicines-recall-aventis-pharma-limited-t-slash-a-sanofi-stemetil-5mg-slash-5ml-syrup-el-22-a-slash-41?utm_medium=email&utm_campaign=govuk-notifications-topic&utm_source=8744b402-2664-40d4-a81b-0fbedeefc431&utm_content=immediately

  Pip Code

     Product Description

 Supplier

Batch Numbers

ALLIANCE DO NOT STOCK

STEMETIL SYRUP 5MG/5ML

 AVENTIS PHARM LTD (T/A SANOFI)

0032

0033

0034

0035

Alliance do not stock the above products so we will not be accepting Customer returns on this recall.

 

For stock control enquiries please contact:

GB-CustomerServices@sanofi.com

Phone number: 0800 854 430

 

For more information or medical information please contact:

uk-medicalinformation@sanofi.com

Phone number: 0800 035 25 25.

 

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.