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
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
- Brand
- Biogenix USA
- 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 2013 | Recall initiated by company | |
| 27 Dec 2013 | Classified by FDA | +114 days |
| 8 Jan 2014 | Published 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
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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