Brew Dr. Uplift Mango Passionfruit, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With…
Recalling firm: BREW DR KOMBUCHA LLC
Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 8, 2021.
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857161008716FDA code information
Best By: 05/20/2021, 07/21/2021, 07/28/2021, 09/16/2021, and 09/20/2021, 9/21/2021. Lot Number: T3435, T3603, T3621, T3746, T3746, and T3747
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Full FDA record and distribution details
Original product description
Brew Dr. Uplift Mango Passionfruit, Yerba Mate *Guayusa * Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00871 6. The label is read in parts: "***MANGO PASSIONFRUIT *** YERBA MATE * GUAYUSA * GREEN TEA *** BREW DR. UPLIFT *** NATURAL CAFFEINE + PROBIOTICS *** CONTAINS 4% JUICE *** INGREDIENTS: Brewed tea (water, yerba mate, green tea, guayusa leaf), cane sugar, mango puree, passionfruit juice, guayusa extract, green tea extract, citric acid, B. coagulans***".
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 857161008716 | tural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00871 6. The label is read in parts: "***MANGO PASSIONFRUIT *** YERBA MATE * GUAYUSA * GREEN TEA *** BREW DR. UPLIFT *** NAT |
| best by | 05/20/2021 | Best By: 05/20/2021, 07/21/2021, 07/28/2021, 09/16/2021, and 09/20/2021, 9/21/2021. Lot Number: T3435, T3603, T3621, T3746, T3746, and T37 |
Original FDA recall reason
Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Recall details
- Recall number
- F-0565-2021
- Event ID
- 87815
- FDA status
- Terminated
- Initiated
- Apr 26, 2021
- Reported
- Jun 2, 2021
- Classified
- May 21, 2021
- Terminated
- Oct 8, 2021
- Quantity
- 4271 flats (12/16 oz. cans per flat)
- Location
- Portland, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
Where it was distributed
Distributed nationwide.
Data updated September 16, 2026. View official FDA data ↗
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