JUICE from the Raw, cashew coffee milk
Everpress Juice recalled this product and the FDA reported the enforcement action on 11 February 2026 as Class I. The recall was initiated by the firm. Under-processed product may contain pathogenic bacteria that could harm to humans.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- JUICE from the Raw, cashew coffee milk
- Reason for recall
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Recalling firm
- Everpress Juice
- Firm location
- Philadelphia, Pennsylvania, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- H-0456-2026
- Quantity
- Unknown
- Distribution
- 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
- Initiated
- 24 July 2025
- Reported by FDA
- 11 February 2026
- Terminated
- 8 April 2026
- Firm notified by
- Product codes
- The firm is in the process of getting the agency the information
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 7 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 7 separate recalls, which almost every published figure does, overstates it by a factor of 7. All 7 of them are listed on this page.
- The recall ran for 8 months, from 24 July 2025 to termination on 8 April 2026. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 21 states, and the FDA published the enforcement report 7 months after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was longer than usual for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Hawaii, Idaho, Montana, Nevada, Oregon, Utah, Washington, Arkansas, Colorado, Illinois, Indiana, Louisiana, Minnesota, Missouri, Mississippi, North Dakota, Oklahoma, South Dakota, Tennessee, Texas, Wyoming. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Process deviation
A process deviation recall means the process ran outside its validated limits: a thermal process that did not reach its time and temperature, a pH that drifted, or a seal that failed.
A preventive controls plan covers a process deviation under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 113
- Thermally processed low-acid foods in hermetically sealed containers: the scheduled process, its establishment by a competent authority, and the records proving every container received it.
- 21 CFR 114
- Acidified foods: the controls on equilibrium pH at or below 4.6, and the process that achieves it.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under milk and dairy, nuts and seeds and beverages and juice. A product can sit in more than one.
Every product in this recall
The FDA opened 7 enforcement records for this one recall, one per product code. This page carries all of them; the 6 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-02-11 | JUICE from the Raw, cashew milk | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, pineapple mint | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, spicy lemonade | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, upbeat | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, sweet greens | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, DETOX GREENS | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
Other milk and dairy recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Everpress Juice
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 6 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-02-11 | JUICE from the Raw, cashew milk | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, pineapple mint | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, spicy lemonade | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, upbeat | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, sweet greens | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
| 2026-02-11 | JUICE from the Raw, DETOX GREENS | Everpress Juice | Under-processed product may contain pathogenic bacteria that could harm to humans. | Class I |
All 7 records for Everpress Juice
All 2026 recalls · All FDA food recall data
21 CFR 113 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.