Recall Radar

Keurig Dr Pepper recalls Diet Snapple Tea Peach Tea: label issue

January 12, 2022 · Keurig Dr Pepper Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallProduct labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Keurig Dr Pepper
Location
Frisco, TX
Reported by FDA
January 12, 2022
Recall started
December 9, 2021
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Nuts, seeds and dried fruit
Reason type
Labeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 7618300314 5. UPC 12 Pack 0 7618300813 3.
    Quantity: 11,970 cases
    Codes: ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)

Where it was distributed

Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Keurig Dr Pepper recalled 1 product, including Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 7618300314 5. UPC 12….

Why was it recalled?

Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

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Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.