Class ITerminatedVoluntary: Firm initiated

Everpress Juice: food recall H-0453-2026

Everpress Juice of Philadelphia, PA recalled JUICE from the Raw, upbeat. Reason: Under-processed product may contain pathogenic bacteria that could harm to humans. The FDA listed it as Class I in its Enforcement Report dated Feb 11, 2026; distribution: Alaska, Arkansas, Arizona, California, Colorado, Hawaii, Idaho, Illinois, Indiana, Louisiana, Minnesota, Missouri, Mississippi, Montana, North Dakota, Nevada, Oklahoma, Oregon, South Dakota, Tennessee, Texas, Utah, Washington, Wyoming.

Record status as published: Terminated (terminated Apr 8, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
JUICE from the Raw, upbeat
Product quantity
Unknown
Reason for recall
Under-processed product may contain pathogenic bacteria that could harm to humans.
Codes, lots and dates on the package
The firm is in the process of getting the agency the information
Distribution pattern
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
Recalling firm
Everpress Juice, Philadelphia, PA
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmJul 24, 2025
Classified by the FDAFeb 2, 2026
Published in the Enforcement ReportFeb 11, 2026
TerminatedApr 8, 2026

Other products in the same recall event

The FDA groups related products under one recall event (event 97330).

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0453-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.