Dierbergs Kitchen House Made Creamy Red Potato Salad packaged in 12 OZ containers UPC 23116800000, and in bulk by pound containers UPC 23...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). 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-0583-2020.
The firm received a recall notice for hardboiled eggs that were potentially contaminated with Listeria monocytogenes. The eggs were subsequently used to manufacture various salad and deli products.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0583-2020.
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 Dierbergs Markets, Inc Corporate Office 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-0583-2020.
Dierbergs Markets, Inc Corporate Office
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.
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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.
Dierbergs Markets, Inc Corporate Office Recall FAQ
Dierbergs Markets, Inc Corporate Office is the subject of a produce safety report: Dierbergs Kitchen House Made Creamy Red Potato Salad packaged in 12 OZ containers UPC 23116800000, and in bulk by pound containers UPC 23.... The notice was published on December 24, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 2,403 units are potentially affected.