a2 Milk Company recalls a2 Platinum Premium infant formula over possible cereulide toxin contamination
The 31.7oz (900g) tins of infant formula for babies up to 12 months may be contaminated with cereulide toxin, which is why the product was recalled.
What to do
The notice does not give instructions. Read the official notice for details.
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.
- Company
- The a2 Milk Company
- Hazard
- Possible contamination with Cereulide toxin.
- Units
- 51,202 units
- Where sold
- The recalled product was distributed throughout the United States.
- FDA classification
- Class I · Terminated
- Classified by FDA
- May 29, 2026
- Recall started
- May 1, 2026
- FDA enforcement report
- June 10, 2026
- Recall closed
- July 31, 2026
- Identifiers
- Codes: Lot # 2210321712 with Expiration Date: 01/14/2027, Lot # 2210324609 with Expiration Date 01/21/2027, Lot # 2210269454 with Expiration Date 07/15/2026
- FDA recall number: H-0891-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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.
- Reason for recall
- Possible contamination with Cereulide toxin.
- Classification
- Class I (Terminated)
- Distribution
- The recalled product was distributed throughout the United States.
- Quantity
- 51,202 units
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