CLASS II Food recall · Reported 12 Feb 2014 · FDA Enforcement Report

an Innophos company Activessence recalled by Triarco Industries

Triarco Industries is recalling an Innophos company Activessence (R) Notice- For Manufacturing Use Only Not for Resale, distributed in California, New York. The recall was initiated on 2 Oct 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes40829
Quantity recalled25 kg

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-1471-2014
FDA event ID
67232
Recalling firm
Triarco Industries, Paterson, NJ
Classification
Class II
Status
Terminated
Recall initiated
2 Oct 2013
FDA classified
4 Feb 2014
Reported
12 Feb 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Other

Timeline

2 Oct 2013Recall initiated by company
4 Feb 2014Classified by FDA+125 days
12 Feb 2014Published 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

Triarco Industries Inc. is recalling product that may have been contaminated with Chloramphenicol.

Product as listed by the FDA

Triarco Industries, LLC an Innophos company Activessence (R) Notice- For Manufacturing Use Only Not for Resale

Where it was distributed

NY, CA

CaliforniaNew York

Questions about this recall

Why was it recalled?

Triarco Industries Inc. is recalling product that may have been contaminated with Chloramphenicol.

Which lots are affected?

40829

Where was it sold?

NY, CA

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.

Other products in this recall event

3 other products · FDA event 67232

This product is part of a recall event; the main page for the event is an Innophos company Multicolor Lightening Drink Granulation recalled.

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