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High RiskFDAfda-F-1132-2016UNDECLARED ALLERGEN

Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.

Category
Units Affected
12
Recall Date
March 18, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1132-2016.

Undeclared soy lecithin in 5 dietary supplements.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1132-2016.

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 Now Foods 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-1132-2016.

NOW Foods

FDA

About the U.S. Food and Drug Administration

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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Now Foods Recall FAQ

Now Foods is the subject of a food safety report: Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.. The notice was published on March 18, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 12 units are potentially affected.