CLASS II Drug recall · Reported 20 Jul 2016 · FDA Enforcement Report

Fuconpo Capsule recalled by Murray International Trading

Murray International Trading Co is recalling Fuconpo Capsule, distributed nationwide in the US. The recall was initiated on 20 Apr 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots
Quantity recalledunknown

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1347-2016
FDA event ID
74017
Recalling firm
Murray International Trading Co, Brooklyn, NY
Classification
Class II
Status
Terminated
Recall initiated
20 Apr 2016
FDA classified
11 Jul 2016
Reported
20 Jul 2016
Type
Voluntary: Firm initiated
Customers notified by
Telephone

Timeline

20 Apr 2016Recall initiated by company
11 Jul 2016Classified by FDA+82 days
20 Jul 2016Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements have labeling that bears drug/disease claims, making them unapproved drugs.

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

FUCONPO CAPSULE, packaged in a 30-count bottle within a box, remaining labeling contains Chinese characters.

Where it was distributed

Nationwide and Puerto Rico

Nationwide Puerto Rico

Questions about this recall

Is Fuconpo Capsule recalled?

Yes. Murray International Trading Co recalled Fuconpo Capsule on 20 Apr 2016. The recall is Class II and its status is Terminated. Recall number D-1347-2016.

Why was it recalled?

Marketed Without An Approved NDA/ANDA: Products marked as dietary supplements have labeling that bears drug/disease claims, making them unapproved drugs.

Which lots are affected?

All lots

Where was it sold?

Nationwide and Puerto Rico

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

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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