CLASS III Food recall · Reported 26 Oct 2016 · FDA Enforcement Report

CardioAdvance recalled by Triceutical Inc./Zhang

Triceutical Inc./Zhang is recalling CardioAdvance, distributed nationwide in the US. The recall was initiated on 10 Oct 2014 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesall lot numbers, all expiration dates
Quantity recalled528 bottles

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-0108-2017
FDA event ID
69241
Recalling firm
Triceutical Inc./Zhang, Farmingdale, NY
Classification
Class III
Status
Terminated
Recall initiated
10 Oct 2014
FDA classified
14 Oct 2016
Reported
26 Oct 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Other

Timeline

10 Oct 2014Recall initiated by company
14 Oct 2016Classified by FDA+735 days
26 Oct 2016Published 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

Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.

Product as listed by the FDA

CardioAdvance

Where it was distributed

*Domestic* - FL, NY, PA, *International*- China

Nationwide FloridaNew YorkPennsylvania

Questions about this recall

Is CardioAdvance recalled?

Yes. Triceutical Inc./Zhang recalled CardioAdvance on 10 Oct 2014. The recall is Class III and its status is Terminated. Recall number F-0108-2017.

Why was it recalled?

Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.

Which lots are affected?

all lot numbers, all expiration dates

Where was it sold?

*Domestic* - FL, NY, PA, *International*- China

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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