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CriticalFDAfda-F-1774-2017LISTERIA

Ham & Cheddar on White Baguette Sandwich 9.2oz retail Plastic packaging Ready to Eat sandwich Keep Refrigerated

⚠ 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.

Category
Units Affected
2,567
Recall Date
February 17, 2017
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1774-2017.

potential contamination with Listeria monocytogenes

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1774-2017.

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 Meijer Distribution, Inc 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-1774-2017.

Meijer Distribution, Inc

FDA

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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📣 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.

How to report to FDAFile a report at FDA

Meijer Distribution, Inc Recall FAQ

Meijer Distribution, Inc is the subject of a food safety report: Ham & Cheddar on White Baguette Sandwich 9.2oz retail Plastic packaging Ready to Eat sandwich Keep Refrigerated. The notice was published on February 17, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 2,567 units are potentially affected.