Summary
The FDA issued a Class I for JUICE from the Raw, sweet greens by Everpress Juice. Reason: Under-processed product may contain pathogenic bacteria that could harm to humans..
Details
Source
Food Recall
External ID
H-0451-2026
Action Date
2026-02-11
Status
Terminated
Category
food
Product Description
JUICE from the Raw, sweet greens
Lot/Code Info: The firm is in the process of getting the agency the information
Quantity Affected: Unknown
Reason for Recall
Under-processed product may contain pathogenic bacteria that could harm to humans.
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-24
Company
Philadelphia, PA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Everpress Juice has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Everpress Juice) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Everpress Juice have FDA actions?
Everpress Juice has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0451-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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