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Class I: serious health riskTerminated

Everpress Juice JUICE from the Raw Recall

JUICE from the Raw, upbeat

Everpress Juice · Philadelphia, PA

Risk level
Class I
Reported by FDA
Feb 11, 2026
Recall ID
H-0453-2026
Check your lot numberHow we source this data

Summary

Everpress Juice recalled JUICE from the Raw starting Jul 24, 2025. The FDA classified it as Class I (serious health risk) and published enforcement report H-0453-2026 on Feb 11, 2026. Reason: Under-processed product may contain pathogenic bacteria that could harm to humans. Status: Terminated.

Why it was recalled

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

Product description

JUICE from the Raw, upbeat

Lot numbers, UPCs & expiration codes

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

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0453-2026
Classification
Class I
Status
Terminated
Recall initiated
Jul 24, 2025
FDA report date
Feb 11, 2026
Quantity
Unknown
Recall type
Voluntary: Firm initiated
Recalling firm
Everpress Juice

Original FDA data

Every field from FDA enforcement report H-0453-2026, exactly as published.

Show all FDA fields
City
Philadelphia
State
PA
Status
Terminated
Country
United States
Event ID
97330
Address
6510 Eastwick Ave
Code information
The firm is in the process of getting the agency the information
Postal code
19142-3311
Report date
Feb 11, 2026
Product type
Food
Recall number
H-0453-2026
Classification
Class I
Recalling firm
Everpress Juice
Product quantity
Unknown
Termination date
Apr 8, 2026
Reason for recall
Under-processed product may contain pathogenic bacteria that could harm to humans.
Voluntary / mandated
Voluntary: Firm initiated
Product description
JUICE from the Raw, upbeat
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
Recall initiation date
Jul 24, 2025
Initial firm notification
E-Mail
Center classification date
Feb 2, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0453-2026, published Feb 11, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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