RecallHawk
Class I Recall

Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information. Cucumb

Delta Fresh LLC.

Summary

The FDA issued a Class I for Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, by Delta Fresh LLC.. Reason: Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak..

Details

Source

Food Recall

External ID

F-0372-2025

Action Date

2025-01-08

Status

Terminated

Category

food

Product Description

Product is a whole, fresh cucumber with no individual packaging, labeling, PLU, or other identifying information. Cucumber weight and size varies. Type of master packaging: 1.PACKAGED IN BULK IN 1 1/9 BUSHEL CARDBOARD BOXES WITH THE DELTA FRESH LABEL; OR 2.PACKAGED IN BULK IN 1 1/9 BUSHEL GENERIC WHITE CARDBOARD BOXES WITH A STICKER THAT PROVIDES THE IMPLICATED GROWER S NAME, AGROTATO, S.A. DE C.V. Net wt: 50 lb UPC: N/A Firm Name & Address listed on label: AGROTATO SA DE CV, BLVD. FRANCISCO EUSEBIO KINO NO. 315, INT. 706, COL. LOMAS DEL PITIC, C.P. 83010, HERMOSILLO, SONORA, MEXICO is listed on the master case. There is no packaging/label/sticker on the cucumbers

Lot/Code Info: Delta Fresh does NOT assign lot information to the shipping container.

Quantity Affected: 6930 cases

Reason for Recall

Potential Salmonella contamination of fresh cucumbers. Associated with an outbreak.

Distribution

Recalled product was distributed to the following states: AZ, CA, IL, MD, MI, MN, NY. and TX.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-11-27

Company

Delta Fresh LLC.

Nogales, AZ

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Delta Fresh LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Delta Fresh LLC. have FDA actions?

This is the only FDA action we have on record for Delta Fresh LLC. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0372-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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