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RECALL RECORD — CLASS IRecall closedH-0452-2026/FDA enforcement
Everpress Juice·Food·Jul 24, 2025

Juice from the Raw, Pineapple Mint

What you need to know

Class I

  • What happened

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

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A process failure may have allowed harmful bacteria to survive in a product that is meant to be safe.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAAK, AZ, CA, HI +20 moreMore food

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Product identification

Source: FDA FOOD

Brand nameEverpress Juice
Recalling firmEverpress JuicePhiladelphia, PA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • The firm is in the process of getting the agency the information
Distribution area
AKAZCAHIIDMTNVORUTWAARCOILINLAMNMOMSNDOKSDTNTXWY

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

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: February 11, 2026
FDA recall numberH-0452-2026

Beyond the headline

The recall, in context

Everpress Juice initiated this food recall on July 24, 2025. The FDA enforcement report states: Under-processed product may contain pathogenic bacteria that could harm to humans. The FDA report lists distribution as: 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.

The FDA enforcement report describes the reason as: Under-processed product may contain pathogenic bacteria that could harm to humans.

Juice from the Raw, Pineapple Mint was made or distributed by Everpress Juice in Philadelphia, PA, United States. This page reflects FDA report H-0452-2026, dated February 11, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a process failure may have allowed harmful bacteria to survive in a product that is meant to be safe.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Juice from the Raw, Pineapple Mint recall?

Everpress Juice recalled Juice from the Raw, Pineapple Mint in an FDA Class I enforcement action reported as H-0452-2026. Under-processed product may contain pathogenic bacteria that could harm to humans.

What are the symptoms of Product safety recall exposure?

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Who is most at risk from Product safety recall?

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

How do I get a refund from Everpress Juice?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0452-2026 and keep the packaging, lot code and proof of purchase if you have them.

Is the Everpress Juice recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0452-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.