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CriticalFDAfda-F-1547-2018SALMONELLA CONTAMINATION

Pious Lion Pure Premium Potent White Maeng DA, Bright Uplifting Energy, 4 oz plastic bag. 833-AVL-KRTM www.piouslion.com

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
110
Recall Date
May 18, 2018
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1547-2018.

The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1547-2018.

Recall ongoing. Follow firm instructions.

✅ 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 Pious Lion 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-1547-2018.

Pious Lion

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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Pious Lion Recall FAQ

Pious Lion is the subject of a food safety report: Pious Lion Pure Premium Potent White Maeng DA, Bright Uplifting Energy, 4 oz plastic bag. 833-AVL-KRTM www.piouslion.com. The notice was published on May 18, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 110 units are potentially affected.