Food recall: Brew Dr. Uplift Blueberry Raspberry Yerba Mate Guayusa, Green Tea, Natural Caffeine With Probiotics. 12/16 oz.…
Class II FDA enforcement event 87815. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Yeast was found in shelf stable 16 oz. aluminum can of Brew Dr. Uplift drink.
Class II, in the words of FDA
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
The recalling firm started this food recall on 26 Apr 2021. The FDA record names a person as the firm, and this site does not show the name. The firm address in the FDA record is in Portland, OR. FDA put the recall in Class II. FDA event 87815 has 3 product records. The first FDA enforcement report date is 2 Jun 2021. The record gives the status Terminated, with the termination date 8 Oct 2021.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Distributed nationwide.
Recalling firm
The name is withheld, Portland, OR.
The FDA record gives the name of a person as the recalling firm. This site does not show the names of persons.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
3 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| 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… | 3439 flats (12/16 oz. cans per flat) | Class II | Terminated | 2 Jun 2021 |
| F-0564-2021 | 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 ***… | 3131 flats (flats (12/16 oz. cans per flat) | Class II | Terminated | 2 Jun 2021 |
| F-0565-2021 | 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 ***… | 4271 flats (12/16 oz. cans per flat) | Class II | Terminated | 2 Jun 2021 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2021
- 463
- Share of these events in Class II
- 57%
- Product records in this event
- 3
Official channels
- FDA enforcement report F-0563-2021The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 87815. https://recallregister.com/fda/ii/87815/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Distributed nationwide.
- What quantity of product is in FDA event 87815?
- The event has 3 product records. The first record gives this quantity:
3439 flats (12/16 oz. cans per flat)
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2021 have the same class?
- 57% of the 463 food events that started in 2021 are in Class II.