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Product Advisory Update
Our Commitments: a2 Platinum® Recall Update
At The a2 Milk Company, food safety and quality is our number one priority. We know parents and caregivers place enormous trust in infant formulas every day. We also understand that this recall may have caused concern, stress and disruption for families. We are deeply sorry.
a2 Platinum® Infant Formula USA Label Product Recall
Boulder, CO – May 2, 2026 – The a2 Milk Company (“a2MC”) has voluntarily recalled three specific batches of its imported a2 Platinum Premium USA label infant formula 0-12 months (“Product”) due to the presence of cereulide. The Product is sold only in the United States.
Cereulide is a heat-stable toxin produced by some strains of the bacterium Bacillus cereus. Illness occurs through the consumption of food contaminated with the toxin and preparing formula with hot water does not eliminate it.
Symptoms typically develop within 30 minutes to six hours of ingestion and most often involve gastrointestinal symptoms such as nausea and vomiting that typically self-resolve within 24 hours. Infants are at greater risk due to their developing immune systems and can experience complications such as dehydration which require medical care.
Product Information
Product Name: a2 Platinum Premium Infant Formula 0-12 months Milk-based powder with Iron
| Packaging Format | Batch Number | Expiration Data |
| 31.7oz tin | 2210269454 | 7/15/2026 |
| 31.7oz tin | 2210324609 | 1/21/2027 |
| 31.7oz tin | 2210321712 | 1/15/2027 |
The batch number and “Use By” (expiration) date are found on the bottom of each tin (refer example below, together with image of product).
The batch number and “Use By” (expiration) date are found on the bottom of each tin (refer to example below, together with image of product).
The Product was distributed nationally through a2MC’s website, Amazon and Meijer stores as part of Operation Fly Formula[1]. Importation rights expired on December 31st, 2025, and the Product has been discontinued and removed from sale prior to the initiation of the recall. The total number of units in the three batches is 63,078 of which an estimated 16,428 units were sold to consumers.
Although no confirmed incidents of illness or harm have been reported, affected batches must not be used.
The recall was initiated by a2MC after cereulide was detected through additional testing of the Product conducted in response to new guidance issued by New Zealand's food regulatory authority. The probable source of cereulide is an ingredient in the Product.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased the Product are recommended to discontinue use of the Product and dispose of it immediately or return to their place of purchase for a refund. If your infant is experiencing symptoms described above, contact your health care provider immediately. To report an illness or adverse event to the FDA, you can:
- Report a Product Problem through SmartHub, or
- Complete and submit a Medwatch report Online at www.fda.gov/medwatch/report.htm, or by Regular Mail or Fax: Download the form from www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
[1] under U.S. Food and Drug Administration enforcement discretion.
