Love & Peas Protein Rich Meal Replacement, Sugar Free, 1 LB 9 OZ (713 G) bag, Nature's Sunshine Products, Inc., Spanish Fork, Utah, 84660...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0792-2021.
The firm was notified by an ingredient supplier of Medium Chain Triglycerides (MCT) that the ingredient potentially contained traces of milk. This affected two of the firm's products that are marketed and sold as vegan and dairy-free.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0792-2021.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Nature's Sunshine Products or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-0792-2021.
NATURE'S SUNSHINE PRODUCTS
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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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.
Nature's Sunshine Products Recall FAQ
Nature's Sunshine Products is the subject of a food safety report: Love & Peas Protein Rich Meal Replacement, Sugar Free, 1 LB 9 OZ (713 G) bag, Nature's Sunshine Products, Inc., Spanish Fork, Utah, 84660.... The notice was published on April 12, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 2,480 units are potentially affected.