Keurig Dr Pepper Rc Cola 12 Oz Aluminum Can Recall: Off Flavor Complaints
Keurig Dr Pepper recalls Rc Cola 12 oz aluminum cans due to consumer complaints of off flavor and aroma. Affected products have production code G1211 CB3U.
Lower-risk recall
Consumer complaints of off flavor and aroma
Contact the company
What happened, in plain English
Keur: Dr Pepper has recalled Rc Cola 12-ounce aluminum cans after consumer complaints about off flavor and aroma. This recall does not involve safety risks but addresses quality issues. Read more at govinfonow.com/recall/14153-keurig-dr-pepper-rc-cola-12-oz-aluminum-can-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/14153-keurig-dr-pepper-rc-cola-12-oz-aluminum-can-recall · Updated August 18, 2026 · FDA enforcement record: FDA #F-0008-2022
Cite this page
“Keurig Dr Pepper Rc Cola 12 Oz Aluminum Can Recall: Off Flavor Complaints.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/14153-keurig-dr-pepper-rc-cola-12-oz-aluminum-can-recall. Based on FDA recall #F-0008-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0008-2022%22&limit=1).
Why it’s dangerous
The recall is due to consumer complaints about off flavor and aroma in the product. This issue does not pose a safety risk but affects product quality.
Who’s affected
Owners of Rc Cola 12 oz aluminum cans with production code G1211 CB3U are affected. Consumers who experienced off flavor or aroma complaints should check their cans.
How to tell if you have this one
Check for Rc Cola 12 oz (355 mL) aluminum cans with production code G1211 CB3U. The product is sold in packs of 12 cans.
- Brand
Keurig Dr Pepper- Category
Food
What to do — step by step
Check Product Code
Look for production code G1211 CB3U on the can.
Where it went and when
Where it was distributed
Distributed in 9 states.
FDA distribution: “West Virginia, Virginia, Ohio, Kentucky, Indiana, Pennsylvania, New Jersey, Tennessee, Georgia.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Georgia, Indiana, Kentucky, New Jersey, Ohio, Pennsylvania, Tennessee, Virginia, West Virginia.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0008-2022 (September 13, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0008-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.