CLASS I Food recall · Reported 3 Jun 2026 · FDA Enforcement Report

Wawa Iced Tea Lemon Pint recalled by Wawa Beverage

Wawa Beverage is recalling Wawa Iced Tea Lemon Pint, distributed in Delaware, Maryland, New Jersey, Pennsylvania, Virginia. The recall was initiated on 2 Apr 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC: 726191018425
Quantity recalledWawa Iced Tea Lemon Pint (16oz) - 15,510

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0855-2026
FDA event ID
98713
Recalling firm
Wawa Beverage, Media, PA
Classification
Class I
Status
Completed
Recall initiated
2 Apr 2026
FDA classified
29 May 2026
Reported
3 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Tea

Timeline

2 Apr 2026Recall initiated by company
29 May 2026Classified by FDA+57 days
3 Jun 2026Published in enforcement report+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Milk Allergen,

Product as listed by the FDA

Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle

Where it was distributed

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

DelawareMarylandNew JerseyPennsylvaniaVirginia

Questions about this recall

Is Wawa Iced Tea Lemon Pint recalled?

Yes. Wawa Beverage recalled Wawa Iced Tea Lemon Pint on 2 Apr 2026. The recall is Class I and its status is Completed. Recall number H-0855-2026.

Why was it recalled?

Undeclared Milk Allergen,

Which lots are affected?

UPC: 726191018425

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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