RecallHawk
Class II Recall

Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack

KEURIG DR PEPPER

Summary

The FDA issued a Class II for Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack by KEURIG DR PEPPER. Reason: Consumer complaints of off flavor and aroma.

Details

Source

Food Recall

External ID

F-0008-2022

Action Date

2021-10-06

Status

Terminated

Category

food

Product Description

Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack

Lot/Code Info: production code of the product is G1211 CB3U

Quantity Affected: 9238 cases

Reason for Recall

Consumer complaints of off flavor and aroma

Distribution

West Virginia, Virginia, Ohio, Kentucky, Indiana, Pennsylvania, New Jersey, Tennessee, Georgia.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-13

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 43 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-0008-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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