Temple Turmeric Recall: Matcha Shots with High Yeast Levels
Temple Turmeric recalls 12-packs and 24-packs of 3 fl oz matcha shots due to high yeast levels. Perishable items must be refrigerated.
Lower-risk recall
High Levels of Yeast
Contact the company
What happened, in plain English
Temple Turmeric is recalling matcha shots that may contain high levels of yeast. This could cause health issues if consumed, so affected customers should stop using the product. Read more at govinfonow.com/recall/16479-temple-turmeric-recall-matcha-shots-with-high-yeast-levels.
Source Summary by GovInfoNow · govinfonow.com/recall/16479-temple-turmeric-recall-matcha-shots-with-high-yeast-levels · Updated October 5, 2026 · FDA enforcement record: FDA #F-0219-2020
Cite this page
“Temple Turmeric Recall: Matcha Shots with High Yeast Levels.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16479-temple-turmeric-recall-matcha-shots-with-high-yeast-levels. Based on FDA recall #F-0219-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0219-2020%22&limit=1).
Why it’s dangerous
The matcha shots contain high levels of yeast, which can cause digestive discomfort or allergic reactions in some people. This is a food safety issue that requires refrigeration to minimize risk.
Who’s affected
Anyone who purchased Temple Turmeric's 3 fl oz matcha shots in 12-packs or 24-packs from 2020. People with sensitive digestive systems may be at higher risk.
How to tell if you have this one
Check for plastic bottles labeled 'TEMPLE PURE PRANA MATCHA+SHOT' in 12-packs or 24-packs. The lot number starts with 01/23/2020.
- Brand
Temple Turmeric- Product
TEMPLE PURE PRANA MATCHA+SHOT; 3 FL OZ (89mL); VITALITY SUPERBOOST; COLD PRESSURED; PERISHABLE KEEP REFRIGERATED- Category
Food
What to do — step by step
Check Product Details
Look for the product name and packaging details on the bottle.
Stop Using if Recalled
If you have the recalled matcha shots, stop using them immediately.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “Direct Distribution to: RI, FL, AR, CA, NJ, TN, CA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, California, Florida, New Jersey, Rhode Island, Tennessee.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class II
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0219-2020 (October 28, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0219-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.