FDA recall record

Sofia Produce Whole cantaloupe, Brand name Rudy 11 count carton, 8 count recall — FDA F-0569-2024

The affected product is being recalled from the marketplace due to possible Salmonella contamination.

Class Iclassification
F-0569-2024official record ID
Dec 13, 2023report date

Recall record at a glance

Official recordF-0569-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSofia Produce, LLC
Report dateDec 13, 2023
Recall initiation dateNov 6, 2023
Quantity18,100 cases
LocationNogales, AZ, United States

Official product description

Whole cantaloupe, Brand name Rudy 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container description; Cardboard containers bearing the Rudy label. The Rudy brand cantaloupes also have an individual PLU sticker placed upon each cantaloupe, PLU sticker # 4050.

Why the product was recalled

The affected product is being recalled from the marketplace due to possible Salmonella contamination.

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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