Media, PA, United States
Wawa Beverage Company recalls
3 recalls recorded since 2018, most recently on 2 April 2026. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)0
Terminated or completed3
Class I (FDA)1
Completed Class I Food
- Recall started
- 2 April 2026
- Reason
- Undeclared Milk Allergen,
- Distribution
- The product has been distributed to the following states: DE, MD, NJ, PA, VA
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- H-0856-2026, H-0857-2026, H-0855-2026, H-0858-2026
- Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
- Wawa Diet Lemonade Pint (16oz), Plastic bottle
- Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle
- Wawa Fruit Punch Pint (16oz), Plastic bottle
Terminated Class II Food
- Recall started
- 17 February 2026
- Terminated
- 7 April 2026
- Reason
- Foreign plastic material discovered on fill line.
- Distribution
- The recalled product was distributed to the following States: NJ,MD, DE, PA
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- H-0585-2026, H-0586-2026, H-0588-2026, H-0587-2026
- Wawa Reduced Fat Milk 2% 16 oz (Pint)
- Wawa Double Dutch Chocolate Milk ,16 oz (Pint) Plastic bottle Store Refrigerated
- Wawa Chocolate Low-fat Milk 16 oz , (Pint) Plastic bottle .Store Refrigerated
- Wawa Cookies & Cream Milk 16 oz (Pint), Plastic bottle Store Refrigerated
Terminated Class II Food
- Recall started
- 23 September 2025
- Terminated
- 17 June 2026
- Reason
- Potential foreign object contamination
- Distribution
- The adulterated product was distributed to the following States: PA,NJ,DE,MD
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- H-0044-2026, H-0043-2026, H-0045-2026
- Wawa Strawberry Milk, Lowfat Milk, 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191015134
- Wawa HVD (Whole) Milk , 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191014403
- Wawa Strawberry Lemonade, 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 007626191018982
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.