Class ITerminated · reported 2026-02-11

JUICE from the Raw, pineapple mint

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, pineapple mint
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-0452-2026
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: E-Mail
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. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 7 of them.
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 a beverage or juice run a median of 6 months, so this one was longer than usual for its category. Juice is the other food with its own HACCP regulation in the United States, 21 CFR part 120, which requires a treatment achieving a 5-log reduction of the pertinent pathogen, and unpasteurised juice recalls are almost always a failure of that step or an exemption misapplied.

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 beverages and juice. A product can sit in more than one.

Other beverages and juice 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.

Reported	Product	Firm	Reason	Class
2026-05-27	Pure Libido Drink 16 oz and 32 oz.	LIQUID BLENZ CORP	May be under-processed resulting in growth of Clostridium botulinum and lists health claims.	Class II
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, cashew coffee milk	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
2025-10-22	Dole Apple Juice (primary package), 15.2 Fl oz., PET, 12 bottles per case, Refrigerate after opening	TROPICANA BRANDS GROUP	A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.	Class II

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, cashew coffee milk	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 access

Recall 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.