CLASS II Food recall · Reported 4 Dec 2013 · FDA Enforcement Report
TriEnza bulk powder recalled by Houston Nutraceuticals
Houston Nutraceuticals is recalling TriEnza bulk powder. The recall was initiated on 8 Nov 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-0381-2014
- FDA event ID
- 66824
- Recalling firm
- Houston Nutraceuticals, Siloam Springs, AR
- Brand
- TriEnza
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Nov 2013
- FDA classified
- 26 Nov 2013
- Reported
- 4 Dec 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 8 Nov 2013 | Recall initiated by company | |
| 26 Nov 2013 | Classified by FDA | +18 days |
| 4 Dec 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 firm is recalling a dietary supplement containing a raw material which may contain >0.3 ppb of chloramphenicol.
Product as listed by the FDA
TriEnza bulk powder distributed in a 5 kilogram polyethylene bag.
Where it was distributed
The product was not distributed domestically. The product was distributed Internationally to Brazil
Questions about this recall
Why was it recalled?
The firm is recalling a dietary supplement containing a raw material which may contain >0.3 ppb of chloramphenicol.
Which lots are affected?
Lot # 83381000
Where was it sold?
The product was not distributed domestically. The product was distributed Internationally to Brazil
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.
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