RecallHawk
Class I Recall

Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 o

Mead Johnson & Company LLC

Summary

The FDA issued a Class I for Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ by Mead Johnson & Company LLC. Reason: Product has the potential to be contaminated with Cronobacter sakazakii..

Details

Source

Food Recall

External ID

F-0809-2024

Action Date

2024-01-24

Status

Terminated

Category

food

Product Description

Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418 or 300871239456 and Use By Date of "1 Jan 2025".

Lot/Code Info: ZL3FHG (12.6 oz cans) ZL3FMH (12.6 oz cans) ZL3FPE (12.6 oz cans) ZL3FQD (12.6 oz cans) ZL3FRW (19.8 oz cans) ZL3FXJ (12.6 oz cans)

Quantity Affected: 1,396,438 cans

Reason for Recall

Product has the potential to be contaminated with Cronobacter sakazakii.

Distribution

Retail stores and medical facilities nationwide and outside the U.S.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-30

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 81 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mead Johnson & Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mead Johnson & Company LLC have FDA actions?

This is the only FDA action we have on record for Mead Johnson & Company LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0809-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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