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CriticalFDAfda-F-0004-2022UNDECLARED ALLERGEN

Duke of Earle X-Large Ham & Cheese, Ham and American Cheese on French Bread. Net Wt. 10.25 oz (297g), UPC 97256 14322, Keep Refrigerated...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
1,124
Recall Date
September 16, 2021
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0004-2022.

Sandwiches may contain undeclared soy and egg.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0004-2022.

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 The Earl Of Sandwiches 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-0004-2022.

The Earl of Sandwiches

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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The Earl Of Sandwiches Recall FAQ

The Earl Of Sandwiches is the subject of a dairy safety report: Duke of Earle X-Large Ham & Cheese, Ham and American Cheese on French Bread. Net Wt. 10.25 oz (297g), UPC 97256 14322, Keep Refrigerated.... The notice was published on September 16, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 1,124 units are potentially affected.