Wawa HVD (Whole) Milk , 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191014403
Summary
The FDA issued a Class II for Wawa HVD (Whole) Milk , 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: by Wawa Beverage Company. Reason: Potential foreign object contamination.
Details
Source
Food Recall
External ID
H-0043-2026
Action Date
2025-10-22
Status
Terminated
Category
food
Product Description
Wawa HVD (Whole) Milk , 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191014403
Lot/Code Info: Code Date: October 9, 2025
Quantity Affected: 154 units
Reason for Recall
Potential foreign object contamination
Distribution
The adulterated product was distributed to the following States: PA,NJ,DE,MD
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-23
Company
Media, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wawa Beverage Company has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wawa Beverage Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wawa Beverage Company have FDA actions?
Wawa Beverage Company has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0043-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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