Skip to main content
High RiskFDAfda-F-1540-2022UNDECLARED ALLERGEN

Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street S...

Units Affected
2,747
Recall Date
July 22, 2022
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1540-2022.

Label declares Whey but does not declare Milk.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1540-2022.

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 Nature's Sunshine Products 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-1540-2022.

NATURE'S SUNSHINE PRODUCTS

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.

Visit FDA.gov →

📣 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.

How to report to FDAFile a report at FDA

Nature's Sunshine Products Recall FAQ

Nature's Sunshine Products is the subject of a snacks & candy safety report: Aivia Whey Protein+ Power Herbs Chocolate, NET WT 1.35 LBS (611 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street S.... The notice was published on July 22, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 2,747 units are potentially affected.