The Recall Desk
HighFDA (Food)·F-3370-2017·Announced 2017-08-23

NatureAll Heart-Plus Dietary Supplement Recalled for Undeclared Soy Allergen

NatureAll is recalling Heart-Plus dietary supplements because they contain soy lecithin, an undeclared allergen. Consumers should stop using the product.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves allergen mislabeling on a common allergen (soy), which corresponds to a severity score of 3 (High) according to the rubric.

Plain-English summary

NatureAll-STF Holding, LLC is voluntarily recalling 598 bottles of Heart-Plus, No. 83, 120 Capsules, Dietary Supplement. The recall is being conducted because the product contains soy lecithin, which is an undeclared allergen. The affected lots are 40800915 and 44300217.

The recalled product was distributed nationwide in the United States, specifically in California, Florida, Georgia, Idaho, Illinois, Indiana, Texas, Utah, Washington, and Wyoming. There are no foreign or government/VA/military consignees listed for this recall.

Consumers who have purchased this product should stop using it immediately. Individuals with a soy allergy should be particularly cautious. For more information, consumers can contact the recalling firm, NatureAll-STF Holding, LLC.

The recalled product

Product
Heart-Plus, No. 83, 120 Capsules, Dietary Supplement
Affected units
598

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot 40800915 & 44300217

Distribution

Distributed nationwide across the United States.

The notice also names 10 states specifically:

Part of a larger recall action

This product is one of 8 recalled by NatureAll-STF Holding, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 8 products in this recall →