Everpress Juice Recalls 'JUICE from the Raw, DETOX GREENS' Due to Potential Pathogenic Bacteria

Source: FDA · AK, AZ, CA, HI, ID, MT, NV, OR, UT, WA, AR, CO, IL, IN, LA, MN, MO, MS, ND, OK, SD, TN, TX, WY

Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.

Everpress Juice has issued a voluntary recall for its 'JUICE from the Raw, DETOX GREENS' product across 24 states due to under-processing concerns that could lead to bacterial contamination.

What this FDA recall tells you, and what most readers miss

This notice was issued by FDA on April 6, 2026 and geographically references AK, AZ, CA, HI, ID, MT, NV, OR, UT, WA, AR, CO, IL, IN, LA, MN, MO, MS, ND, OK, SD, TN, TX, WY. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.

Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.

What Happened

Everpress Juice, located in Philadelphia, Pennsylvania, has initiated a voluntary recall of its "JUICE from the Raw, DETOX GREENS" product. The recall was classified as Class I by the FDA, indicating a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. The recall was prompted because the juice was under-processed, which may allow for the presence of pathogenic bacteria that could be harmful to humans.

Which Products Are Affected

The recall affects the following product:

  • Product Name: JUICE from the Raw, DETOX GREENS
  • Recall Number: H-0450-2026
  • Quantity: Unknown
  • Code Information: The firm is currently in the process of providing specific lot codes and identification information to the FDA.

Distribution Area: The product was distributed in the following states: Alaska, Arizona, California, Hawaii, Idaho, Montana, Nevada, Oregon, Utah, Washington, Arkansas, Colorado, Illinois, Indiana, Louisiana, Minnesota, Missouri, Mississippi, North Dakota, Oklahoma, South Dakota, Tennessee, Texas, and Wyoming.

What You Should Do

Consumers who have purchased "JUICE from the Raw, DETOX GREENS" in the affected states are advised not to consume the product. While specific return or refund instructions were not provided in the initial enforcement report, consumers typically should dispose of the product or return it to the place of purchase.

Why This Matters

Under-processed food and beverage products can harbor dangerous pathogens. Consuming products contaminated with pathogenic bacteria poses a high risk of serious illness or infection.

Source

Information provided by the FDA (Event ID: 97330).

Original source: FDA Official Notice ↗

All FDA Recalls →

Frequently Asked Questions

Common questions about this FDA recall.

What is this FDA recall about?
Everpress Juice has issued a voluntary recall for its 'JUICE from the Raw, DETOX GREENS' product across 24 states due to under-processing concerns that could lead to bacterial contamination.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "high" severity. Take precautions and monitor for updates.
What area is affected?
This alert affects AK, AZ, CA, HI, ID, MT, NV, OR, UT, WA, AR, CO, IL, IN, LA, MN, MO, MS, ND, OK, SD, TN, TX, WY. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.