HP Hood Blue Diamond Almond Breeze Almond Milk Recall: Milk Allergen Detected
HP Hood recalls Blue Diamond Almond Breeze Almond Milk due to testing positive for milk allergen. Consumers should check product codes and contact HP Hood for details.
Lower-risk recall
HP Hood LLC, has initiated a recall of Blue Diamond Almond Breeze Almond Milk, Half Gallon, because the product tested positive for milk allergen.
Contact the company
What happened, in plain English
HP Hood is recalling Blue Diamond Almond Breeze Al: Half Gallon almond milk because it tested positive for milk allergen. This poses a risk for people with milk allergies. Read more at govinfonow.com/recall/18782-hp-hood-blue-diamond-almond-breeze-almond-milk-recall-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/18782-hp-hood-blue-diamond-almond-breeze-almond-milk-recall-milk · Updated October 6, 2026 · FDA enforcement record: FDA #F-1832-2018
Cite this page
“HP Hood Blue Diamond Almond Breeze Almond Milk Recall: Milk Allergen Detected.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18782-hp-hood-blue-diamond-almond-breeze-almond-milk-recall-milk. Based on FDA recall #F-1832-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1832-2018%22&limit=1).
Why it’s dangerous
The almond milk tested positive for milk allergen, which can cause allergic reactions in sensitive individuals. This is a food safety issue for those with milk allergies.
Who’s affected
People with milk allergies are at risk from this almond milk product. The recall affects consumers who purchased the specific half-gallon size.
How to tell if you have this one
Check for the product code on the label: SEP 02 18 HH:MM (military time) H5 L# (1 or 2) 51-4109. The recall applies to half-gallon Blue Diamond Almond Breeze Almond Milk.
- Brand
HP Hood- Category
Food
What to do — step by step
Check Product Code
Look for the product code on the label: SEP 02 18 HH:MM (military time) H5 L# (1 or 2) 51-4109.
How this recall unfolded
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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 #F-1832-2018 (August 1, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1832-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.