CLASS I Food recall · Reported 28 Jun 2017 · FDA Enforcement Report
NutriHeal Optimal Cholesterol Traditional Vegetarian Blend recalled
Herbmed USA Company is recalling NutriHeal Optimal Cholesterol Traditional Vegetarian Blend Herbal Supplement. The recall was initiated on 26 May 2017 and the FDA has classified it as Class I.
Check your package
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-2387-2017
- FDA event ID
- 77322
- Recalling firm
- Herbmed USA Company, Jericho, NY
- Brand
- NutriHeal Optimal
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 26 May 2017
- FDA classified
- 21 Jun 2017
- Reported
- 28 Jun 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Milk
- Product category
- Herbal Supplements
Timeline
| 26 May 2017 | Recall initiated by company | |
| 21 Jun 2017 | Classified by FDA | +26 days |
| 28 Jun 2017 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains undeclared milk.
Product as listed by the FDA
NutriHeal OPTIMAL CHOLESTEROL Traditional Vegetarian Blend Herbal Supplement, 60 Tablets. Distributed By: Herbmed USA Company Inc.
Where it was distributed
China
Questions about this recall
Is NutriHeal Optimal Cholesterol Traditional Vegetarian Blend Herbal Supplement recalled?
Yes. Herbmed USA Company recalled NutriHeal Optimal Cholesterol Traditional Vegetarian Blend Herbal Supplement on 26 May 2017. The recall is Class I and its status is Terminated. Recall number F-2387-2017.
Why was it recalled?
Product contains undeclared milk.
Which lots are affected?
Lot#0401916 Exp 04/2019
Where was it sold?
China
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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