RecallHawk
Class I Recall

Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle

Wawa Beverage Company

Summary

The FDA issued a Class I for Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle by Wawa Beverage Company. Reason: Undeclared Milk Allergen,.

Details

Source

Food Recall

External ID

H-0855-2026

Action Date

2026-06-03

Status

Ongoing

Category

food

Product Description

Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle

Lot/Code Info: UPC: 726191018425

Quantity Affected: Wawa Iced Tea Lemon Pint (16oz) - 15,510

Reason for Recall

Undeclared Milk Allergen,

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-02

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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-0855-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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