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CriticalFDAfda-F-0585-2024SALMONELLA CONTAMINATION

Mixed Fruit Products that contain Cantaloupe, Honeydew, and Red Grapes, Identified with the following Item ID and Description. 1. 8366...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
10
Recall Date
November 24, 2023
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0585-2024.

Cantaloupe containing products may be contaminated with Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0585-2024.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Cut Fruit Express, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0585-2024.

Cut Fruit Express, Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Cut Fruit Express, Inc. Recall FAQ

Cut Fruit Express, Inc. is the subject of a produce safety report: Mixed Fruit Products that contain Cantaloupe, Honeydew, and Red Grapes, Identified with the following Item ID and Description. 1. 8366.... The notice was published on November 24, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 10 units are potentially affected.