Small Ranch Tray with Dip, NET WT, 21.9 OZ (1 lb 5.9 OZ) 620g, Dist. By: Renaissance Food Group LLC 4322 Moreland Ave. Conley, GA 30288, ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (other). 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-0023-2023.
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0023-2023.
Recall ongoing. Follow firm instructions.
✅ 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 Renaissance Food Group 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-0023-2023.
Renaissance Food Group
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.
Renaissance Food Group Recall FAQ
Renaissance Food Group is the subject of a food safety report: Small Ranch Tray with Dip, NET WT, 21.9 OZ (1 lb 5.9 OZ) 620g, Dist. By: Renaissance Food Group LLC 4322 Moreland Ave. Conley, GA 30288, .... The notice was published on September 12, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 120 units are potentially affected.