CLASS III Food recall · Reported 8 May 2019 · FDA Enforcement Report

Iced Tea Less Sugar recalled by Wawa

Wawa is recalling Iced Tea Less Sugar, distributed in Delaware, Pennsylvania. The recall was initiated on 12 Apr 2019 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesApril 29, 2019 (APR/29/19)
Quantity recalled710 cases were distributed.

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
F-1326-2019
FDA event ID
82643
Recalling firm
Wawa, Media, PA
Brand
Iced
Classification
Class III
Status
Terminated
Recall initiated
12 Apr 2019
FDA classified
2 May 2019
Reported
8 May 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Labeling Errors
Product category
Tea

Timeline

12 Apr 2019Recall initiated by company
2 May 2019Classified by FDA+20 days
8 May 2019Published in enforcement report+6 days

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

Reason for recall

WAWA has initiated a recall of Wawa Iced Tea Less Sugar, Net weight/number of units per package: 12 FL OZ. , Package type: Bottle Units per case: 24, Expiration date: April 29, 2019 (APR/29/19) because of mislabeling. The label reads does not list required phenylketonuria warning and ingredient listing does not list Aspartame.

Product as listed by the FDA

Wawa Iced Tea Less Sugar, Net weight/number of units per package: 12 FL OZ. , Package type: Bottle Units per case: 24, Expiration date: April 29, 2019 (APR/29/19)

Where it was distributed

Product was distributed to Pennsylvania and Delaware.

DelawarePennsylvania

Questions about this recall

Why was it recalled?

WAWA has initiated a recall of Wawa Iced Tea Less Sugar, Net weight/number of units per package: 12 FL OZ. , Package type: Bottle Units per case: 24, Expiration date: April 29, 2019 (APR/29/19) because of mislabeling. The label reads does not list required phenylketonuria warning and ingredient listing does not list Aspartame.

Which lots are affected?

April 29, 2019 (APR/29/19)

Where was it sold?

Product was distributed to Pennsylvania and Delaware.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 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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