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Class III: unlikely to cause harmTerminated

Red Bull Energy Drink Recall

Red Bull Energy Drink, 8

Red Bull North America Inc. · Santa Monica, CA

Risk level
Class III
Reported by FDA
Dec 5, 2018
Recall ID
F-0671-2019
Check your lot numberHow we source this data

Summary

Red Bull North America recalled Red Bull Energy Drink starting Nov 2, 2018. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-0671-2019 on Dec 5, 2018. Reason: 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. Status: Terminated.

Why it was 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.

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.

Lot numbers, UPCs & expiration codes

BATCH/LOT NUMBER: 1639377 AND 1639378; USE BY DATES: 05/16/2020 AND 05/18/2020, RESPECTIVELY C. PRODUCTION TIME STAMP RANGE (CAN): a. BATCH 1639377 TIME STAMP 14:00 14:48 b. BATCH 1639378 TIME STAMP 14:48 15:20, 17:00 17:40, 19:20 20:10, 21:10 21:15 D. PRODUCTION TIME STAMP RANGE (CASE LABELS) a. BATCH 1639377 TIME STAMP 14:15 14:58 b. BATCH 1639378 TIME STAMP 14:58 15:40, 17:10 17:50, 19:30 20:20, 21:20 21:25

Where it was sold

DC's in CA, NV, AZ, HI, UT

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0671-2019
Classification
Class III
Status
Terminated
Recall initiated
Nov 2, 2018
FDA report date
Dec 5, 2018
Quantity
BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS
Recall type
Voluntary: Firm initiated
Recalling firm
Red Bull North America Inc.

Original FDA data

Every field from FDA enforcement report F-0671-2019, exactly as published.

Show all FDA fields
City
Santa Monica
State
CA
Status
Terminated
Country
United States
Event ID
81503
Address
1630 Stewart St
Code information
BATCH/LOT NUMBER: 1639377 AND 1639378; USE BY DATES: 05/16/2020 AND 05/18/2020, RESPECTIVELY C. PRODUCTION TIME STAMP RANGE (CAN): a. BATCH 1639377 TIME STAMP 14:00 14:48 b. BATCH 1639378 TIME STAMP 14:48 15:20, 17:00 17:40, 19:20 20:10, 21:10 21:15 D. PRODUCTION TIME STAMP RANGE (CASE LABELS) a. BATCH 1639377 TIME STAMP 14:15 14:58 b. BATCH 1639378 TIME STAMP 14:58 15:40, 17:10 17:50, 19:30 20:20, 21:20 21:25
Postal code
90404-4015
Report date
Dec 5, 2018
Product type
Food
Recall number
F-0671-2019
Classification
Class III
Recalling firm
Red Bull North America Inc.
Product quantity
BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS
Termination date
May 9, 2019
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.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
DC's in CA, NV, AZ, HI, UT
Recall initiation date
Nov 2, 2018
Initial firm notification
Letter
Center classification date
Nov 28, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0671-2019, published Dec 5, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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