CLASS I Drug recall · Reported 18 Jun 2014 · FDA Enforcement Report

Super Fat Burning Bomb Capsules, 400 mg, supplied recalled by MyNicNaxs

MyNicNaxs is recalling Super Fat Burning Bomb Capsules, 400 mg, supplied, distributed nationwide in the US. The recall was initiated on 24 Jan 2014 and the FDA has classified it as Class I.

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-1374-2014
FDA event ID
67471
Recalling firm
MyNicNaxs, Deltona, FL
Classification
Class I
Status
Terminated
Recall initiated
24 Jan 2014
FDA classified
12 Jun 2014
Reported
18 Jun 2014
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Labeling Errors

Timeline

24 Jan 2014Recall initiated by company
12 Jun 2014Classified by FDA+139 days
18 Jun 2014Published in enforcement report+6 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: Product was found to contain undeclared active pharmaceutical ingredients: Phenolphthalein and N-desmethylsibutramine

Product as listed by the FDA

Super Fat Burning Bomb Capsules, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: Phenolphthalein and N-desmethylsibutramine

Which lots are affected?

ALL LOTS

Where was it sold?

Nationwide

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 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 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.

Other products in this recall event

9 other products · FDA event 67471

This product is part of a recall event; the main page for the event is Fruta BIO, supplied recalled by MyNicNaxs.

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