FDA recall record

Wawa Net weight/number of units per package: 12 FL OZ recall — FDA F-1326-2019

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,…

Class IIIclassification
F-1326-2019official record ID
May 8, 2019report date

Recall record at a glance

Official recordF-1326-2019
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmWawa, Inc.
Report dateMay 8, 2019
Recall initiation dateApr 12, 2019
Quantity710 cases were distributed.
LocationMedia, PA, United States

Official product description

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)

Why the product was 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.

Distribution information

Product was distributed to Pennsylvania and Delaware.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.