← FDA ENFORCEMENT
H-0453-2026Class I

Everpress Juice

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Everpress Juice
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2026-02-11
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
Firm state
PA
Product quantity
Unknown
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Under-processed product may contain pathogenic bacteria that could harm to humans.

Product description

JUICE from the Raw, upbeat

Code / lot info

The firm is in the process of getting the agency the information

Other recalls SPEQ maps to Environmental Monitoring
See all Environmental Monitoring recalls →

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →