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CriticalFDAfda-F-0109-2020LISTERIA

Market Sandwich Dill Egg Salad on Classic White Bread, Net Wt. 5.0 oz. (142g) UPC: 41433-02669 Keep Refrigerated. Deli Express, Eden ...

⚠ 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.

Units Affected
331,692
Recall Date
October 1, 2019
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0109-2020.

Various sandwiches have the potential to be contaminated with Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0109-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact E.a. Sween Co. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0109-2020.

E.A. Sween Co.

FDA

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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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📣 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.

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E.a. Sween Co. Recall FAQ

E.a. Sween Co. is the subject of a bakery & grains safety report: Market Sandwich Dill Egg Salad on Classic White Bread, Net Wt. 5.0 oz. (142g) UPC: 41433-02669 Keep Refrigerated. Deli Express, Eden .... The notice was published on October 1, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 331,692 units are potentially affected.