Food Recall Check
Class I · High risk Terminated Initiated May 1, 2026 (5 months ago)

a2 Platinum Premium infant formula Milk-based Powder with Iron recall

Recalled by The a2 Milk Company · Boulder, CO, United States

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

Why it was recalled

Possible contamination with Cereulide toxin.

Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.

What was recalled

a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12 months). Condition: shelf stable product Type of packaging: metal tin with plastic dust cap. Net weight: 31.7oz (900gm). UPC: 813267020335. Firm name listed on label: The a2 Milk Company. 4909 Pearl East Circle, Suite 300 Boulder CO 80301.

Quantity: 51,202 units

Food: Milk & dairy 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.

Lot # 2210321712 with Expiration Date: 01/14/2027, Lot # 2210324609 with Expiration Date 01/21/2027, Lot # 2210269454 with Expiration Date 07/15/2026

Where it was sold

Nationwide.

FDA's distribution note: The recalled product was distributed throughout the United States.

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
The a2 Milk Company
Initiated by
Voluntary: Firm initiated
Recall initiated
May 1, 2026
In FDA report of
Jun 10, 2026
Terminated
Jul 31, 2026
FDA recall number
H-0891-2026 · event 98887
Official record
FDA enforcement report search

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