Recall map → All recalls → F-0563-2021
Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa, Green Tea, Natural Caffeine With Probiotics. 12/16 oz. aluminum cans per cardboard flat. UPC 8 57161 00867 9. The label is read in parts: "***BLUEBERRY RASPBERRY ***YERBA MATE * GUAYUSA * GREEN TEA***BREW DR UPLIFT *** NATURAL CAFFEINE + PROBIOTICS *** CONTAIN 2% JUICE *** INGREDIENTS: Brewed tea (water, yerba mate, green tea elderberry currant, hibiscus, guayusa leaf, goji berry, strawberry, raspberry blueberry), cane sugar, blueberry juice, guayusa extract, green tea extract, citric acid, B. coagulans***". BREW DR KOMBUCHA LLC · reported 2021-06-02
Terminated This recall has been closed out by the agency.
- Reason for recall
- Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
- Classification
- Class II
- Recall initiated
- 2021-04-26
- Reported by the agency
- 2021-06-02
- Closed out (terminated)
- 2021-10-08
- Recalling firm
- BREW DR KOMBUCHA LLC
Portland, OR
United StatesThis is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
- Distribution (the agency's own words)
- Distributed nationwide.
- States we parsed from that text
- AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WYour expansion
The agency wrote a broader phrase; these state names are ours, not theirs. Parse method nationwide, confidence high.
- Food category
- Beverages Dietary supplements Produce (fruit & vegetables)derived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
- Recall type
- Voluntary: Firm initiated
- Recall number
- F-0563-2021
View this record at the agency source →
This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.