The affected product is being recalled from the marketplace due to possible 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 FDAIN, ORMore food
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Our information corresponding to Lot Codes is our Order Number. Order Numbers: 0128556, 0128624, 0128630, 0128632, 0128640, 0128643, 0128644, 0128646, 0128648, 0128651, 0128656, 0128669, 0128680, 0128682, 0128683, 0128700, 0225200, 0225201, 0225206, 0225214, 0225219, 0225222, 0225226, 0225227, 0225228, 0419611, 0419629, 0419630, 0419636, 0419671, 0419688, 0419693, 0419696, 0419697, 0419704, 0419710, 0419718, 0419772, 0516255, 0516268, 0516271, 0516279, 0516301, 0612143, 0612144, 0612148, 0612154, 0612156, 0612158, 0612171, 0612190, 0612191, 0612197, 0612198, 0612209, 0612225 Above Order Numbers are all those associated with all shipments which could have contained products related to the Canadian Recall. On 11/14/2023 TruFresh expanded the recall to include the following Sales order numbers associated with the lots that tested positive in Canada. 128663, 128712, 128713, 128662, 128680, 225252, 225231, 419719, 419721, 419828, 419803, 612235 612273
Distribution area
INOR
Customers are located in the United States & Canada. There is no distribution to US Government agencies or departments. Product was distributed to consignees in the following states: California, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Ohio, South Dakota, Tennessee, Texas, Virginia, West Virginia, Wisconsin and Washington D.C.
United States, Canada
Quantity affected
12, 706 boxes original recall. 5, 649 boxes for the expanded recall. Totaling 18, 335 boxes.
Recall initiation
FDA report date: December 13, 2023
FDA recall number
F-0568-2024
Beyond the headline
The recall, in context
Sofia Produce, L.l.c. initiated this food recall on November 6, 2023. The FDA enforcement report states: The affected product is being recalled from the marketplace due to possible Salmonella contamination. The FDA report lists distribution as: Customers are located in the United States & Canada. There is no distribution to US Government agencies or departments. Product was distributed to consignees in the following states: California, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maryland, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Ohio, South Dakota, Tennessee, Texas, Virginia, West Virginia, Wisconsin and Washington D.C.
The FDA enforcement report describes the reason as: The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Whole Cantaloupe, Brand Name Malichita 11 Count Carton, 8 Count Carton, 9 Count Carton, 15… was made or distributed by Sofia Produce, L.l.c. in Nogales, AZ, United States. This page reflects FDA report F-0568-2024, 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
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the UPC and lot code against the table above.
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
1Stop using or eating the affected product and keep it away from children and pets.
2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
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
4 answers
What is the Whole Cantaloupe, Brand Name Malichita 11 Count Carton, 8 Count Carton, 9 Count Carton, 15… recall?
Sofia Produce, L.l.c. recalled Whole Cantaloupe, Brand Name Malichita 11 Count Carton, 8 Count Carton, 9 Count Carton, 15… in an FDA Class I enforcement action reported as F-0568-2024. The affected product is being recalled from the marketplace due to possible Salmonella contamination.
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.
Is the Sofia Produce, L.l.c. 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-0568-2024. 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.