Alert

Company Led Recall – Nutramigen LGG Stage 1 and Stage 2 Infant Formula

As a precaution Reckitt are recalling certain batches of the Nutramigen LGG Stage 1 and stage 2 due to an isolated overseas sample of the product testing positive for Cronobacter sakazakii. Both products are foods used for special medical purposes for infants, ordinarily to be used under medical supervision.

Ref: FSA-PRIN-01-2024

Company name: Reckitt

Product description: Nutramigen LGG Stage 1 and Stage 2 infant formula

Details of the affected batches:

Regulatory Batch

Code Description

Expiry Date

ZL3F7D

Nutramigen LGG Stage 1, 400 g

1st July 2025

ZL3FAA

Nutramigen LGG Stage 2, 400 g

1st July 2025

ZL3FDM

Nutramigen LGG Stage 2, 400 g

1st July 2025

Brief description of problem:

Reckitt is recalling the above products and have contacted all stores and pharmacies that are supplying these products. The company has also issued a recall notice to its customers. There is a potential presence of Cronobacter sakazakii.

Symptoms caused by Cronobacter sakazakii usually include fever and diarrhoea, and in severe cases may lead to sepsis or meningitis which include symptoms in infants including poor feeding, irritability, temperature changes, jaundice (yellow skin and whites of the eyes) and abnormal breaths and movements.

Advice to consumers:

If you have purchased or been prescribed any of the above product batches, do not feed it to your baby and return to the place of purchase or dispensing. If you have additional questions, please contact Reckitt on 01895 230575. If you have any concerns about the health of your baby, please seek medical advice.

Advice to Healthcare Professionals:

Stop supplying the above batches immediately. Quarantine all remaining stock and any patient returns and return it to your supplier using your supplier’s approved process.

Company contacts for further information:

Careline freephone number +44 (0)1895 230575 

Email ConsumerNutrition_GB@rb.com

To access the FSA notice: Nutramigen LCG Stage 1 and 2 recall