CLASS II Food recall · Reported 23 Aug 2017 · FDA Enforcement Report

Heart-Plus, No. 83, Dietary Supplement recalled by NatureAll-STF Holding

NatureAll-STF Holding is recalling Heart-Plus, No. 83, Dietary Supplement, distributed nationwide in the US. The recall was initiated on 26 Jul 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 40800915 & 44300217
Quantity recalled598 bottles.

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-3370-2017
FDA event ID
77831
Recalling firm
NatureAll-STF Holding, Salt Lake City, UT
Classification
Class II
Status
Terminated
Recall initiated
26 Jul 2017
FDA classified
14 Aug 2017
Reported
23 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Dietary Supplements

Timeline

26 Jul 2017Recall initiated by company
14 Aug 2017Classified by FDA+19 days
23 Aug 2017Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergens: soy (lecithin)

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Heart-Plus, No. 83, 120 Capsules, Dietary Supplement

Where it was distributed

Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

Nationwide CaliforniaFloridaGeorgiaIdahoIllinoisIndianaTexasUtahVirginiaWashingtonWyoming

Questions about this recall

Why was it recalled?

Undeclared allergens: soy (lecithin)

Which lots are affected?

Lot 40800915 & 44300217

Where was it sold?

Nationwide, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

7 other products · FDA event 77831

This product is part of a recall event; the main page for the event is Acidophilus-Plus, No. 102, Dietary Supplement recalled.

More recalls from NatureAll-STF Holding

All 8

Other Dietary Supplements recalls

All 733