RecallHawk
Class II Recall

Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 76183

KEURIG DR PEPPER

Summary

The FDA issued a Class II for Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: Febru by KEURIG DR PEPPER. Reason: Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error..

Details

Source

Food Recall

External ID

F-0361-2022

Action Date

2022-01-12

Status

Terminated

Category

food

Product Description

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.

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

Quantity Affected: 11,970 cases

Reason for Recall

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

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2021-12-09

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 11 food recalls issued in the same week, part of 204 food-related FDA actions this month.

KEURIG DR PEPPER has 7 FDA actions in our database, including 7 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KEURIG DR PEPPER) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does KEURIG DR PEPPER have FDA actions?

KEURIG DR PEPPER has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0361-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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