Whole Foods Market Mid-Atlantic Kitchen Tom Yom Soup Recall

Why it was recalled

Ready to eat soup lists whey in the ingredient statement, but the product does not declare milk as the source for the allergen.

Product description

Tom Yom Soup, 24 oz. plastic cups, packed 6 cups\cardboard case, and labeled in part ***Manufactured by Whole Foods Market, Landover, MD 20785***UPC 00000601467***

Lot numbers, UPCs & expiration codes

Use by 4/8/14

Where it was sold

Product was distributed to MD, NJ, OH, VA, KY, PA, and Washington, D.C.

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-1743-2014
Classification: Class I
Status: Terminated
Recall initiated: Feb 19, 2014
FDA report date: Apr 9, 2014
Quantity: 504 cups
Recall type: Voluntary: Firm initiated
Recalling firm: Whole Foods Market Mid-Atlantic Kitchen

Original FDA data

Every field from FDA enforcement report F-1743-2014, exactly as published.

Show all FDA fields

City: Landover
State: MD
Status: Terminated
Country: United States
Event ID: 67577
Address: 1521 Cabin Branch Dr
Code information: Use by 4/8/14
Postal code: 20785-3816
Report date: Apr 9, 2014
Product type: Food
Recall number: F-1743-2014
Classification: Class I
Recalling firm: Whole Foods Market Mid-Atlantic Kitchen
Product quantity: 504 cups
Termination date: Apr 8, 2014
Reason for recall: Ready to eat soup lists whey in the ingredient statement, but the product does not declare milk as the source for the allergen.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Tom Yom Soup, 24 oz. plastic cups, packed 6 cups\cardboard case, and labeled in part ***Manufactured by Whole Foods Market, Landover, MD 20785***UPC 00000601467***
Distribution pattern: Product was distributed to MD, NJ, OH, VA, KY, PA, and Washington, D.C.
Recall initiation date: Feb 19, 2014
Initial firm notification: E-Mail
Center classification date: Apr 3, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1743-2014, published Apr 9, 2014. 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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