Class ITerminatedVoluntary: Firm initiated
The a2 Milk Company: food recall H-0891-2026
The a2 Milk Company of Boulder, CO recalled a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12… Reason: Possible contamination with Cereulide toxin. The FDA listed it as Class I in its Enforcement Report dated Jun 10, 2026; distribution: nationwide.
Record status as published: Terminated (terminated Jul 31, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 51,202 units
- Reason for recall
- Possible contamination with Cereulide toxin.
- Codes, lots and dates on the 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
- Distribution pattern
- The recalled product was distributed throughout the United States.
- Recalling firm
- The a2 Milk Company, Boulder, CO
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 1, 2026 |
| Classified by the FDA | May 29, 2026 |
| Published in the Enforcement Report | Jun 10, 2026 |
| Terminated | Jul 31, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0891-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.