CLASS I Food recall · Reported 18 Sep 2013 · FDA Enforcement Report
Clinical LIVE Dietary Supplement Immune Support 694.325 mg recalled
Reaction Nutrition is recalling Clinical LIVE Dietary Supplement Immune Support 694.325 mg, distributed nationwide in the US. The recall was initiated on 7 Nov 2012 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-1879-2013
- FDA event ID
- 65982
- Recalling firm
- Reaction Nutrition, Carnegie, PA
- Brand
- Clinical LIVE
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 7 Nov 2012
- FDA classified
- 10 Sep 2013
- Reported
- 18 Sep 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Allergens
- Product category
- Dietary Supplements
Timeline
| 7 Nov 2012 | Recall initiated by company | |
| 10 Sep 2013 | Classified by FDA | +307 days |
| 18 Sep 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The product contained an undeclared allergen, Colostrum, which is considered a dairy product and therefore requires an allergen statement on the label.
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
Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules Distributed by Reaction Nutrition, LLC., Carnegie, PA.
Where it was distributed
Nationwide.
Questions about this recall
Why was it recalled?
The product contained an undeclared allergen, Colostrum, which is considered a dairy product and therefore requires an allergen statement on the label.
Which lots are affected?
lot # PB0091512, exp. date 8/2014, UPC code 283333900111
Where was it sold?
Nationwide.
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 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.
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