Rootify
CompaniesFAQ
Hp Hood Llc
Recall · Class III2012-10-30Terminated

Contains almond without saying so on the label, which matters if you are allergic to it.

Product labeled as Unsweetened Vanilla Blue Diamond Almond Breeze Almond milk may contain chocolate flavored Almondmilk ( undeclared ingredients: cocoa and evaporated cane juice).

Above, in the agency’s own words. The line before it is our plain-English summary — how we word these.

Issued by the US Food and Drug Administration, naming Hp Hood Llc.

What the notice covered

Blue Diamond Almond Breeze Almond milk Half Gallon (1.89 L) Paper Carton UPC: 4157005618

Quoted from the record as published. If a product is not described here, this notice does not tell us whether it was affected.

What Class III means

The FDA’s least serious class: use of the product is not likely to cause adverse health consequences. Often a labelling or packaging fault.

This is the agency’s own definition of the class. We do not assign classes and we do not rank them against each other.

The record

Agency
US Food and Drug Administration (FDA)
Reference number
F-0742-2013
Kind of action
Recall
Dated
2012-10-30
Terminated
2013-09-10
Status on the record
Terminated
We read it
2026-10-01

Regulates most packaged food, drugs and devices. Its recall records are published weekly in the Enforcement Report.

Products we matched to this notice

We have not matched this notice to any product in our database — usually because it named no barcode we hold. Products may still have been affected.

How we are treating it

Nobody has yet assessed whether this notice concerns the products we track for this company, so it is not shown on product pages.

The government record

The FDA publishes this notice through its enforcement API, so the link below returns raw JSON rather than a readable page. It is the primary record and we cite it as such; everything above is our transcription of it.

https://api.fda.gov/food/enforcement.json?search=recall_number:"F-0742-2013"

To see it in the FDA’s own words, search the reference number F-0742-2013 in the Search the FDA Enforcement Report. The FDA publishes no direct link to an individual recall.

How we source every record on this site