Food Recall Check
Class I · High risk Terminated Initiated Dec 30, 2023 (3 years ago)

Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans recall

Recalled by Mead Johnson & Company LLC · Zeeland, MI, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product has the potential to be contaminated with Cronobacter sakazakii.

Pathogen: Cronobacter

A bacterium of particular concern in powdered infant formula.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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".

Quantity: 1,396,438 cans

Food: Baby food & infant formula

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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)

Where it was sold

Nationwide.

FDA's distribution note: Retail stores and medical facilities nationwide and outside the U.S.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Mead Johnson & Company LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 30, 2023
In FDA report of
Jan 24, 2024
Terminated
Aug 13, 2025
FDA recall number
F-0809-2024 · event 93718
Official record
FDA enforcement report search

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