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FDA source record Class I Terminated

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....

Recall Date: 2024-11-27 Recalling Firm: Delta Fresh LLC. Record Ref: F-0372-2025

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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.... and names Delta Fresh LLC. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Delta Fresh LLC.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2024-11-27
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

FDA public announcements can appear before an enforcement report is classified, so an empty classification does not mean the notice is unimportant.

Product Description & Identification

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

Reason for Recall / Hazard Identified

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

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

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

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0372-2025
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record