Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cups 3330-3 Fruit Mi...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0578-2024.
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0578-2024.
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 Vinyard Fruit & Vegetable Co., 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-0578-2024.
Vinyard Fruit & Vegetable Co., 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.
Vinyard Fruit & Vegetable Co., Llc Recall FAQ
Vinyard Fruit & Vegetable Co., Llc is the subject of a produce safety report: Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cups 3330-3 Fruit Mi.... The notice was published on November 10, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 599 units are potentially affected.