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FDA Food recall · Reported December 5, 2018

Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainamide, Calcium Pantothenate, Pyridoxine HCL, Vitamin B12, Natural and artificial Flavors, colors. UPC CODES: 6 11269 99100 0 (ON THE CANS) AND 61126991246 (ON THE CASES) distributed by Red Bull, N.A. Inc., Santa Monica, CA Made in Austria.

Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.

Recall #
F-0671-2019
Affected scope
BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS
Initiated
November 2, 2018
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Red Bull North America Inc. recalled Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Gl… - a low-severity action.

Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Gl… was recalled by Red Bull North America Inc. in December 5, 2018. Reason: Investigation of complaints of off taste color and taste found that the product contained 3 times the level o…. Check the official notice for the remedy. Verify recall #F-0671-2019 with the FDA Food before acting.

The recall

Red Bull North America Inc. issued this low-severity FDA Food recall-Investigation of complaints of off taste color and taste found that the product contained 3 times the level o….

Low
severity level
Class III
classification
December 5, 2018
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0671-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainamide, Calcium Pantothenate, Pyridoxine HCL, Vitamin B12, Natural and artificial Flavors, colors. UPC CODES: 6 11269 99100 0 (ON THE CANS) AND 61126991246 (ON THE CASES) distributed by Red Bull, N.A. Inc., Santa Monica, CA Made in Austria.

Reason for recall

Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number F-0671-2019
Date reported December 5, 2018
Date initiated November 2, 2018
Recalling firm Red Bull North America Inc.
Firm location Santa Monica, CA
Affected scope BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS
Distribution DC's in CA, NV, AZ, HI, UT

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-0671-2019) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainamide, Calcium Pantothenate, Pyridoxine HCL, Vitamin B12, Natural and artificial Flavors, colors. UPC CODES: 6 11269 99100 0 (ON THE CANS) AND 61126991246 (ON THE CASES) distributed by Red Bull, N.A. Inc., Santa Monica, CA Made in Austria.. Recalled by Red Bull North America Inc.. Units affected: BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS.
Why was this product recalled?
Investigation of complaints of off taste color and taste found that the product contained 3 times the level of the primary ingredients than is specified in the product formulation.
Which agency issued this recall?
This recall was issued by the FDA Food on December 5, 2018. Severity: Low. Recall number: F-0671-2019.
Where was the recalled product distributed?
Distribution: DC's in CA, NV, AZ, HI, UT.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

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This recall: FDA Food, reported December 5, 2018. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026