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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Beverages

KEURIG DR PEPPER: Rc Cola Recalled Due to Off Flavor and Aroma

Agency Publication Date: September 27, 2021
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Summary

Keurig Dr Pepper has recalled approximately 9,238 cases of Rc Cola 12 oz (355 mL) cans due to consumer complaints of an off flavor and aroma. The recall affects 12-packs of aluminum cans with the specific production code G1211 CB3U. Consumers should not consume the product and should return it to the store where it was purchased for a full refund.

Risk

The product does not meet quality standards, resulting in an unpleasant taste and smell that prompted consumer complaints. While no illnesses have been reported, the off-flavor and aroma indicate a quality defect that makes the product unsuitable for consumption.

What You Should Do

  1. Identify if you have the affected product by checking for 12-packs of 12 oz (355 mL) Rc Cola aluminum cans.
  2. Look for the production code G1211 CB3U printed on the product packaging to confirm it is part of the recall.
  3. Stop using and do not consume any of the affected soda cans immediately.
  4. Return the product to the place of purchase for a full refund or contact Keurig Dr Pepper for further instructions.
  5. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

💰Full Refund

Return to the place of purchase for a full refund or contact the manufacturer for further instructions

How to: Return the affected 12-packs of Rc Cola to the retailer where they were bought for a complete refund.

Affected Products

Product: Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a pack
Item Code:
F-0008-2022
Lot Numbers:
G1211 CB3U

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88723
Status: Resolved
Manufacturer: KEURIG DR PEPPER
Sold By: retailers
Manufactured In: United States
Units Affected: 9238 cases
Distributed To: West Virginia, Virginia, Ohio, Kentucky, Indiana, Pennsylvania, New Jersey, Tennessee, Georgia
Agency Last Updated: October 5, 2021

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.