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

Bella Vi BTrim MAX Dietary Supplement capsules recalled

Pure Edge Nutrition is recalling Bella Vi BTrim MAX Dietary Supplement capsules, www.BellaViProducts.com, distributed nationwide in the US. The recall was initiated on 10 Oct 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codeslot # BTX13 EXP: 2015/08/15

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-1366-2014
FDA event ID: 67810
Recalling firm: Pure Edge Nutrition, Toms River, NJ
Classification: Class I
Status: Terminated
Recall initiated: 10 Oct 2013
FDA classified: 12 Jun 2014
Reported: 18 Jun 2014
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Labeling Errors

Timeline

10 Oct 2013	Recall initiated by company
12 Jun 2014	Classified by FDA	+245 days
18 Jun 2014	Published 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 sibutramine & phenolphthalein

Product as listed by the FDA

Bella Vi BTrim MAX Dietary Supplement capsules, 60 count bottles, www.BellaViProducts.com, distributed by Pure Edge Nutrition, LLC, Toms River, NJ

Where it was distributed

Nationwide

Questions about this recall

Why was it recalled?

Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein

Which lots are affected?

lot # BTX13 EXP: 2015/08/15

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 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

5 other products · FDA event 67810

This product is part of a recall event; the main page for the event is Bella Vi eXtreme Accelerator Dietary Supplement Capsules recalled.

Reported	Class	Recall	Company	Reason	Where
18 Jun 2014	CLASS I	Bella Vi eXtreme Accelerator Dietary Supplement Capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014	CLASS I	Bella Vi Amp'd UP Advanced Weight Loss Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014	CLASS I	Bella Vi BTrim Ultimate Boost Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014	CLASS I	Bella Vi Insane Bee Pollen Dietary Supplement Capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014	CLASS I	Bella Vi Insane Amp'd Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide

More recalls from Pure Edge Nutrition

All 6

Reported	Class	Recall	Company	Reason	Where
18 Jun 2014Drug	CLASS I	Bella Vi Insane Amp'd Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014Drug	CLASS I	Bella Vi Insane Bee Pollen Dietary Supplement Capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014Drug	CLASS I	Bella Vi BTrim Ultimate Boost Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014Drug	CLASS I	Bella Vi Amp'd UP Advanced Weight Loss Dietary Supplement capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide
18 Jun 2014Drug	CLASS I	Bella Vi eXtreme Accelerator Dietary Supplement Capsules recalled	Pure Edge Nutrition	Labeling Errors	Nationwide