Whole Foods Market Mid-Atlantic Kitchen Pimento Cheese Recall

Why it was recalled

Pimento cheese was mislabeled with an ingredient list, which did not declare the presence of mayonnaise, containing egg sub-ingredient.

Product description

Pimento Cheese, packaged in 7 oz. plastic containers, and labeled in part ***Made by Whole Foods Market, Landover, MD 20785***UPC: 000000234801

Lot numbers, UPCs & expiration codes

Use by 07/29/13

Where it was sold

The product was distributed to Kentucky, Maryland, Pennsylvania, Ohio, Virginia, Washington D.C. and New Jersey.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1746-2013
Classification: Class I
Status: Terminated
Recall initiated: Jul 16, 2013
FDA report date: Aug 7, 2013
Quantity: 624 units
Recall type: Voluntary: Firm initiated
Recalling firm: Whole Foods Market Mid-Atlantic Kitchen

Original FDA data

Every field from FDA enforcement report F-1746-2013, exactly as published.

Show all FDA fields

City: Landover
State: MD
Status: Terminated
Country: United States
Event ID: 65737
Address: 1521 Cabin Branch Dr
Code information: Use by 07/29/13
Postal code: 20785-3816
Report date: Aug 7, 2013
Product type: Food
Recall number: F-1746-2013
Classification: Class I
Recalling firm: Whole Foods Market Mid-Atlantic Kitchen
Product quantity: 624 units
Termination date: Sep 11, 2013
Reason for recall: Pimento cheese was mislabeled with an ingredient list, which did not declare the presence of mayonnaise, containing egg sub-ingredient.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Pimento Cheese, packaged in 7 oz. plastic containers, and labeled in part ***Made by Whole Foods Market, Landover, MD 20785***UPC: 000000234801
Distribution pattern: The product was distributed to Kentucky, Maryland, Pennsylvania, Ohio, Virginia, Washington D.C. and New Jersey.
Recall initiation date: Jul 16, 2013
Initial firm notification: E-Mail
Center classification date: Jul 26, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1746-2013, published Aug 7, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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