CANTALOUPE, HONEYDEW, PINEAPPLE AND RED GRAPE, DIP: H.Brooks 33478 FRUIT TRAY w/dip 2.5# Net Wt 40 oz (1134 g) 292 2 per case UPC# 0...
⚠ 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-0034-2013.
Cut Fruit Express, Inc processed cantaloupe that was later recalled by the supplier DFI Marketing due to a positive Salmonella sample.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0034-2013.
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 Cut Fruit Express, Inc. 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-0034-2013.
Cut Fruit Express, Inc.
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.
Cut Fruit Express, Inc. Recall FAQ
Cut Fruit Express, Inc. is the subject of a produce safety report: CANTALOUPE, HONEYDEW, PINEAPPLE AND RED GRAPE, DIP: H.Brooks 33478 FRUIT TRAY w/dip 2.5# Net Wt 40 oz (1134 g) 292 2 per case UPC# 0.... The notice was published on September 13, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 372 units are potentially affected.