RECALL RECORD — CLASS IRecall closedF-0667-2024/FDA enforcement

Mixed Fruit Cup, Clam-shell Container

What you need to know

Class I
  • What happened

    Potential Salmonella contamination.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

  • 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 FDAIA, MN, ND, WIMore food

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Product identification

Source: FDA FOOD

Brand nameFreshpoint Bix Produce Company, LLC
Recalling firmFreshpoint Bix Produce Company, LLCLittle Canada, MN, United States
UPC / barcodes
8 46709 00463 1
Lot / date codes
  • Lot number / Sales Order #: 1. 05942067, , 05942889, 05946790, 05947528, 05949236, 05949354, 05949366, 05949372, 05949373, 05949376, 05951560, 05952880, 05953348, 05953778, 05953831, 05953997, 05954868, 05955822, 05956330, 05956584, 05957076, 05958221, 05958558, 05958781, 05958814, 05958829, 05958913, 05958928, 05958953, 05959665, 05959666, 05959744, 05959851, 05959915, 05959939, 05960064, 05960080, 05960851, 05961031, 05961088, 05961219, 05961302, 05961424, 05961463, 05961588, 05961592. 2. 05953154, 05953565, 05953680, 05954099, 05954280, 05954380. Sell By 10/25/2023 and 10/26/2023.
Distribution area
IAMNNDWI

IA, MN, ND, WI

United States

Quantity affected432 units
Recall initiationFDA report date: December 13, 2023
FDA recall numberF-0667-2024

Beyond the headline

The recall, in context

Freshpoint Bix Produce Company, LLC initiated this food recall on November 17, 2023. The FDA enforcement report states: Potential Salmonella contamination. The FDA report lists distribution as: IA, MN, ND, WI.

The FDA enforcement report describes the reason as: Potential Salmonella contamination.

Mixed Fruit Cup, Clam-shell Container was made or distributed by Freshpoint Bix Produce Company, LLC in Little Canada, MN, United States. This page reflects FDA report F-0667-2024, dated December 13, 2023.

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 bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

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 UPC and lot code 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

Salmonella

Symptoms to watch for

Diarrhea, fever, abdominal cramps, nausea and sometimes vomiting. Symptoms can be severe in young children, older adults and immunocompromised people.

When symptoms may appear

Usually 6 hours to 6 days after exposure; illness often lasts 4 to 7 days.

Higher-risk groups

Children under 5, adults over 65, pregnant people and anyone with a weakened immune system are more likely to develop severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

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 Mixed Fruit Cup, Clam-shell Container recall?

Freshpoint Bix Produce Company, LLC recalled Mixed Fruit Cup, Clam-shell Container in an FDA Class I enforcement action reported as F-0667-2024. Potential Salmonella contamination.

What are the symptoms of Salmonella exposure?

Diarrhea, fever, abdominal cramps, nausea and sometimes vomiting. Symptoms can be severe in young children, older adults and immunocompromised people.

How quickly can Salmonella symptoms appear?

Usually 6 hours to 6 days after exposure; illness often lasts 4 to 7 days.

Who is most at risk from Salmonella?

Children under 5, adults over 65, pregnant people and anyone with a weakened immune system are more likely to develop severe illness.

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 affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Freshpoint Bix Produce Company, LLC?

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 F-0667-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the Freshpoint Bix Produce Company, LLC 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 F-0667-2024. 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.