CLASS I Drug recall · Reported 19 Mar 2014 · FDA Enforcement Report
BEST Slim, Dietary Supplement recalled by CTV Best Group
CTV Best Group is recalling BEST Slim, Dietary Supplement, 100% Natural Weight Loss Pill, 40 Pills per, distributed nationwide in the US. The recall was initiated on 1 Aug 2013 and the FDA has classified it as Class I.
Check your package
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-1154-2014
- FDA event ID
- 65900
- Recalling firm
- CTV Best Group, Duluth, GA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 1 Aug 2013
- FDA classified
- 12 Mar 2014
- Reported
- 19 Mar 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 1 Aug 2013 | Recall initiated by company | |
| 12 Mar 2014 | Classified by FDA | +223 days |
| 19 Mar 2014 | Published in enforcement report | +7 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 contains an undeclared drug, sibutramine, making it an unapproved new drug.
Product as listed by the FDA
BEST Slim, Dietary Supplement, 100% Natural Weight Loss Pill, 40 Pills per bottle, Distributed by CTV Best Group Inc., P.O. Box 956452, Duluth, GA 30095.
Where it was distributed
Nationwide and Australia, Canada.
Questions about this recall
Is BEST Slim, Dietary Supplement, 100% Natural Weight Loss Pill, 40 Pills per recalled?
Yes. CTV Best Group recalled BEST Slim, Dietary Supplement, 100% Natural Weight Loss Pill, 40 Pills per on 1 Aug 2013. The recall is Class I and its status is Terminated. Recall number D-1154-2014.
Why was it recalled?
Marketed without an Approved NDA/ANDA: Product contains an undeclared drug, sibutramine, making it an unapproved new drug.
Which lots are affected?
All lots (lot 109400, Exp 12/31/2016)
Where was it sold?
Nationwide and Australia, Canada.
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.