Severity
Low
LowClass IIITerminated
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.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
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 FDA Food action (record #F-0671-2019) was formally reported on December 5, 2018, with the manufacturer initiating the action on November 2, 2018. It is classified under Low severity (Class III), with a current status of Terminated. Red Bull North America Inc. is listed as the recalling firm, operating out of Santa Monica, CA. Federal records list the affected scope as BATCH # 1639377 48,456 CANS, BATCH # 1639378 146,160 CANS.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: DC's in CA, NV, AZ, HI, UT. Distribution scope 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 - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
BATCH # 1639377 48,456 CANS, BATCH # 1639378 146,160 CANS
Related Recalls
6
0 from same agency
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
| 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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0671-2019) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
· 2026-07-02
CPSC Moderate
Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Heat Pumps Due to Risk of Serious Injury f…
· 2026-06-25
CPSC Moderate
Arizer Solo III Portable Vaporizers Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Imported by…
· 2026-06-18
FDA Devices Moderate
GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used i…
GE Medical Systems Information Technologies Inc · 2026-06-03
FDA Devices Critical
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit…
Medline Industries, LP · 2026-06-03
Compare this recall with Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Ser… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 5, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.