CLASS I Food recall · Reported 11 Feb 2026 · FDA Enforcement Report

Juice from the Raw, cashew coffee milk recalled by Everpress Juice

Everpress Juice is recalling Juice from the Raw, cashew coffee milk, distributed in 24 states. The recall was initiated on 24 Jul 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesThe firm is in the process of getting the agency the information

Quantity recalledUnknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: H-0456-2026
FDA event ID: 97330
Recalling firm: Everpress Juice, Philadelphia, PA
Classification: Class I
Status: Terminated
Recall initiated: 24 Jul 2025
FDA classified: 2 Feb 2026
Reported: 11 Feb 2026
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Product category: Milk

Timeline

24 Jul 2025	Recall initiated by company
2 Feb 2026	Classified by FDA	+193 days
11 Feb 2026	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Under-processed product may contain pathogenic bacteria that could harm to humans.

Product as listed by the FDA

JUICE from the Raw, cashew coffee milk

Where it was distributed

The adulterated product was distributed the following states : AK,AZ CA, HI,ID,MT,NV,OR,UT,WA,AR,CO,IL,IN,LA,MN,MO,MS,ND,OK,SD,TN,TX,WY

Alaska Arkansas Arizona California Colorado Hawaii Idaho Illinois Indiana Louisiana Minnesota Missouri Mississippi Montana North Dakota Nevada Oklahoma Oregon South Dakota Tennessee

Questions about this recall

Is Juice from the Raw, cashew coffee milk recalled?

Yes. Everpress Juice recalled Juice from the Raw, cashew coffee milk on 24 Jul 2025. The recall is Class I and its status is Terminated. Recall number H-0456-2026.

Why was it recalled?

Under-processed product may contain pathogenic bacteria that could harm to humans.

Which lots are affected?

The firm is in the process of getting the agency the information

Where was it sold?

The adulterated product was distributed the following states : AK,AZ CA, HI,ID,MT,NV,OR,UT,WA,AR,CO,IL,IN,LA,MN,MO,MS,ND,OK,SD,TN,TX,WY

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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