CLASS II Food recall · Reported 12 Jan 2022 · FDA Enforcement Report

Diet Snapple Tea Peach Tea recalled by Keurig Dr Pepper

Keurig DR Pepper is recalling Diet Snapple Tea Peach Tea, distributed nationwide in the US. The recall was initiated on 9 Dec 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)
Quantity recalled11,970 cases

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-0361-2022
FDA event ID
89191
Recalling firm
Keurig DR Pepper, Frisco, TX
Classification
Class II
Status
Terminated
Recall initiated
9 Dec 2021
FDA classified
5 Jan 2022
Reported
12 Jan 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects
Product category
Tea

Timeline

9 Dec 2021Recall initiated by company
5 Jan 2022Classified by FDA+27 days
12 Jan 2022Published in enforcement report+7 days

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

Reason for recall

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

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

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

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)

Where was it sold?

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

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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