Uplift Blood Orange Kombucha (Brew Dr) – yeast contamination (2021)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Brew Dr. Uplift Blood Orange Lemon, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00870 9. The label is read in parts: "***BLOOD ORANGE LEMON *** YERBA MATE * GUAYUSA * GREEN TEA***BREW DR. UPLIFT *** NATURAL CAFFEINE + PROBIOTICS *** CONTAINS 2% JUICE *** INGREDIENTS: Brewed tea (water, yerba mate, green tea, guayusa leaf), cane sugar, lemon juice, blood orange puree, guayusa extract, green tea extract, citrict aci
Brand
BREW DR KOMBUCHA LLC
Lot Codes / Batch Numbers
Best By: 05/24/2021, 07/28/2021, 07/29/2021, 08/26/2021, and 09/09/2021. Lot Number: T3436, T3620, T3620, T3673, and T3673.
Products Sold
Best By: 05/24/2021, 07/28/2021, 07/29/2021, 08/26/2021, and 09/09/2021. Lot Number: T3436, T3620, T3620, T3673, and T3673.
BREW DR KOMBUCHA LLC is recalling Brew Dr. Uplift Blood Orange Lemon, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotic due to Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026