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FDA recall record

Red Bull Energy Drink, 8.4 Fl. oz. (250 mL) Ingredient: Carbonated water, Sucrose, Glucose, Citric Acid, Taurine, Sodium Bicarbonate, Magnesium, Carbonate Caffeine, Nicainam...

Recall F-0671-2019Class IIITerminatedNovember 2, 2018

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of May 9, 2019. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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. A. , Santa Monica, CA Made in Austria.

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.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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. A. , Santa Monica, CA Made in Austria.

Code information listed by FDA

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

Distribution and firm information

Recalling firm listed by FDA: Red Bull North America Inc.

Firm location listed by FDA: Santa Monica, CA, United States

Distribution reported by FDA: DC's in CA, NV, AZ, HI, UT

Product quantity listed by FDA: BATCH # 1639377  48,456 CANS, BATCH # 1639378  146,160 CANS

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.