CLASS II Food recall · Reported 8 Jan 2014 · FDA Enforcement Report

Biogenix USA Vitalikor capsules recalled by Mira Health Products

Mira Health Products is recalling Biogenix USA Vitalikor capsules, distributed in Florida, Georgia, North Carolina, New Jersey. The recall was initiated on 4 Sep 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots within expiry and distributed prior to August 2013
Quantity recalledunknown

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-1326-2014
FDA event ID
65916
Recalling firm
Mira Health Products, Farmingdale, NY
Classification
Class II
Status
Terminated
Recall initiated
4 Sep 2013
FDA classified
27 Dec 2013
Reported
8 Jan 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Dietary Supplements

Timeline

4 Sep 2013Recall initiated by company
27 Dec 2013Classified by FDA+114 days
8 Jan 2014Published in enforcement report+12 days

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

Reason for recall

The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.

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

Biogenix USA Vitalikor capsules, packaged in plastic bottles with 40 capsules per bottle.

Where it was distributed

GA, FL, NC, possibly NJ and New Zealand

FloridaGeorgiaNorth CarolinaNew Jersey

Questions about this recall

Is Biogenix USA Vitalikor capsules recalled?

Yes. Mira Health Products recalled Biogenix USA Vitalikor capsules on 4 Sep 2013. The recall is Class II and its status is Terminated. Recall number F-1326-2014.

Why was it recalled?

The dietary supplements have the potential to be contaminated with undeclared steroids, pharmaceutical ingredients and/or chemical additives due to lack of GMPs.

Which lots are affected?

All lots within expiry and distributed prior to August 2013

Where was it sold?

GA, FL, NC, possibly NJ and New Zealand

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 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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