FDA recall H-0451-2026 · Feb 11, 2026
Everpress Juice: JUICE from the Raw recall
Product
JUICE from the Raw, sweet greens
Reason for recall
Under-processed product may contain pathogenic bacteria that could harm to humans.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Terminated
- Codes, lots and dates
- The firm is in the process of getting the agency the information
- 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
- Recalling firm
- Everpress Juice, Philadelphia, PA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-07-24
Source: openFDA enforcement record H-0451-2026 · search recall number H-0451-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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