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Lower risk Food recall · FDA · Published May 1, 2026

a2 Platinum Premium Infant Formula Recall: Possible Cereulide Toxin Contamination

The a2 Milk Company recalls a2 Platinum Premium infant formula (31.7oz) due to possible contamination with Cereulide toxin. This could cause illness in infants. Consumers should check lot numbers on the metal tin packaging.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0891-2026Fooda2 Milk Company ›
Official FDA recall photos · click to enlarge
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Contact the company

Recalling firmThe a2 Milk Company4909 Pearl East Cir Ste 300 · Boulder, CO 80301-6100
✎ GovInfoNow plain-language explainer

The a2 Milk Company is recalling a2 Platinum Premium infant formula powder for possible contamination with Cereulide toxin. This could cause illness in infants who consume the product. The recall affects specific lot numbers with expiration dates up to January 2027. Read more at govinfonow.com/recall/6411-a2-platinum-premium-infant-formula-recall-possible-cereulide-toxin-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/6411-a2-platinum-premium-infant-formula-recall-possible-cereulide-toxin-contamination · Updated August 10, 2026 · Official notice: FDA #H-0891-2026

Cite this page

“a2 Platinum Premium Infant Formula Recall: Possible Cereulide Toxin Contamination.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6411-a2-platinum-premium-infant-formula-recall-possible-cereulide-toxin-contamination. Based on FDA recall #H-0891-2026.

The FDA announced on May 1, 2026, that The a2 Milk Company is voluntarily recalling a2 Platinum Premium infant formula due to possible contamination with Cereulide toxin. Owners should stop using the product immediately.

How to tell if you have it

  • a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g)
  • UPC: 813267020335
  • Lot # 2210321712, Expiration Date: 01/14/2027
  • Lot # 2210324609, Expiration Date: 01/21/2027
  • Lot # 2210269454, Expiration Date: 07/15/2026

The hazard

The recalled product may be contaminated with Cereulide toxin. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar infant formula products include the Nara Organics Infant Formula Recall (2026-06-13) and the ByHeart Infant Formula Cans Contaminated with Botulinum Toxin - Recall (2025-11-08). Additional recent recalls in this category include the Wellnov Liposomal D3+B12 Spray Recall: Bacterial Pathogen Risk (2026-04-23).

How to tell if you have this one

Check the metal tin packaging for lot numbers: 2210321712 (expires 01/14/2027), 2210324609 (expires 01/21/2027), or 2210269454 (expires 07/15/2026). The product is labeled as a2 Platinum Premium infant formula with iron.

  • Brand
    a2 Milk Company
  • Product
    a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for the lot number on the metal tin packaging: 2210321712, 2210324609, or 2210269454.

  2. Discard Recalled Product

    If the product has a recalled lot number, discard it immediately and do not use it.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “The recalled product was distributed throughout the United States.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: May 1, 202612. FDA classified it Class I: May 29, 202623. Published in FDA’s Enforcement Report: Jun 10, 202634. FDA terminated the recall: Jul 31, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0891-2026 (May 1, 2026)
  • Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA