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Lower risk Food recall · FDA · Published November 2, 2018

Red Bull Recall: Off Taste and Color Due to Ingredient Levels

Red Bull North America recalls specific batches of 8.4 oz energy drinks due to off taste, color, and excessive ingredient levels.

🇺🇸 FDA recall #F-0671-2019FoodRed Bull ›
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Recalling firmRed Bull North America Inc.1630 Stewart St · Santa Monica, CA 90404-4015
✎ GovInfoNow plain-language explainer

What happened, in plain English

Red Bull North America Inc. is recalling specific batches of 8.4 Fl. oz. (250 mL) Red Bull Energy Drink because the product contained three times the level of primary ingredients specified in the formulation. This error resulted in complaints regarding off taste and color. The recall affects products distributed to distribution centers in California, Nevada, Arizona, Hawaii, and Utah. Read more at govinfonow.com/recall/18100-red-bull-recall-off-taste-and-color-due-to-ingredient.

Source Summary by GovInfoNow · govinfonow.com/recall/18100-red-bull-recall-off-taste-and-color-due-to-ingredient · Updated October 11, 2026 · FDA enforcement record: FDA #F-0671-2019

Cite this page

“Red Bull Recall: Off Taste and Color Due to Ingredient Levels.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18100-red-bull-recall-off-taste-and-color-due-to-ingredient. Based on FDA recall #F-0671-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0671-2019%22&limit=1).

Why it’s dangerous

The investigation found that the product contained three times the level of primary ingredients compared to the standard formulation. This deviation caused the energy drink to have an off taste and unusual color, which are quality control issues rather than immediate health hazards like toxicity or contamination.

Who’s affected

Consumers who purchased Red Bull Energy Drink 8.4 oz cans from distribution centers in CA, NV, AZ, HI, or UT between the production dates listed. The primary risk is sensory dissatisfaction (off taste and color) rather than physical injury.

How to tell if you have this one

Check your cans for UPC codes 6 11269 99100 0 (on cans) or 61126991246 (on cases). Verify the batch/lot numbers are 1639377 or 1639378. Check the use-by dates of 05/16/2020 or 05/18/2020, and look for specific production time stamps on the can or case label corresponding to those batches.

  • Brand
    Red Bull
  • Product
    Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine
  • Category
    Food

Where it went and when

Where it was distributed

Distributed in 5 states and D.C..

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: yesHITexas: not listedTXFlorida: not listedFL

FDA distribution: “DC's in CA, NV, AZ, HI, UT” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, District of Columbia, Hawaii, Nevada, Utah.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Nov 2, 201812. FDA classified it Class III: Nov 28, 201823. Published in FDA’s Enforcement Report: Dec 5, 201834. FDA terminated the recall: May 9, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. 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-0671-2019 (November 2, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0671-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA