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Class I: serious health riskCompleted

Wawa Diet Lemonade Pint Recall

Wawa Diet Lemonade Pint (16oz), Plastic bottle

Wawa Beverage Company · Media, PA

Risk level
Class I
Reported by FDA
Jun 3, 2026
Recall ID
H-0857-2026
Check your lot numberHow we source this data

Summary

Wawa Beverage recalled Wawa Diet Lemonade Pint starting Apr 2, 2026. The FDA classified it as Class I (serious health risk) and published enforcement report H-0857-2026 on Jun 3, 2026. Reason: Undeclared Milk Allergen,. Status: Completed.

Why it was recalled

Undeclared Milk Allergen,

Product description

Wawa Diet Lemonade Pint (16oz), Plastic bottle

Lot numbers, UPCs & expiration codes

UPC: 726191055901

Where it was sold

The product has been distributed to the following states: DE, MD, NJ, PA, VA

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
H-0857-2026
Classification
Class I
Status
Completed
Recall initiated
Apr 2, 2026
FDA report date
Jun 3, 2026
Quantity
Wawa Diet Lemonade Pint (16oz) - 374
Recall type
Voluntary: Firm initiated
Recalling firm
Wawa Beverage Company

Original FDA data

Every field from FDA enforcement report H-0857-2026, exactly as published.

Show all FDA fields
City
Media
State
PA
Status
Completed
Country
United States
Event ID
98713
Address
1393 W Baltimore Pike
Code information
UPC: 726191055901
Postal code
19063-5502
Report date
Jun 3, 2026
Product type
Food
Recall number
H-0857-2026
Classification
Class I
Recalling firm
Wawa Beverage Company
Product quantity
Wawa Diet Lemonade Pint (16oz) - 374
Reason for recall
Undeclared Milk Allergen,
Voluntary / mandated
Voluntary: Firm initiated
Product description
Wawa Diet Lemonade Pint (16oz), Plastic bottle
Distribution pattern
The product has been distributed to the following states: DE, MD, NJ, PA, VA
Recall initiation date
Apr 2, 2026
Initial firm notification
E-Mail
Center classification date
May 29, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0857-2026, published Jun 3, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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