Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit Bowl 40oz, Seaso...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (laceration). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0772-2024.
The select fresh-cut products were made from whole cantaloupe subject to a previously announced voluntary recall initiated by Sofia Produce, LLC dba Trufresh. The whole cantaloupe may have the potential to be contaminated with Salmonella.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0772-2024.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Cf Dallas Llc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-0772-2024.
CF Dallas LLC
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 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.
Cf Dallas Llc Recall FAQ
Cf Dallas Llc is the subject of a produce safety report: Seasonal Blend 10oz, Seasonal Blend 16oz, Seasonal Blend 42oz , Melon Trio 16oz, Melon Mix 32oz, Fruit Blend 16oz, Fruit Bowl 40oz, Seaso.... The notice was published on November 20, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 27,998 units are potentially affected.