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High RiskFDAfda-F-0219-2020OTHER

TEMPLE PURE PRANA MATCHA+SHOT; 3 FL OZ (89mL); VITALITY SUPERBOOST; COLD PRESSURED; PERISHABLE KEEP REFRIGERATED; plastic bottles in 12 p...

Category
Units Affected
18,732
Recall Date
October 28, 2019
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0219-2020.

High Levels of Yeast

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0219-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Temple Turmeric Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0219-2020.

Temple Turmeric Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Temple Turmeric Inc. Recall FAQ

Temple Turmeric Inc. is the subject of a food safety report: TEMPLE PURE PRANA MATCHA+SHOT; 3 FL OZ (89mL); VITALITY SUPERBOOST; COLD PRESSURED; PERISHABLE KEEP REFRIGERATED; plastic bottles in 12 p.... The notice was published on October 28, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 18,732 units are potentially affected.