CLASS I Drug recall · Reported 28 Dec 2016 · FDA Enforcement Report
Skinny Bee Diet capsules, 500 mg recalled by Love My Tru Body
Love My Tru Body is recalling Skinny Bee Diet capsules, 500 mg, distributed nationwide in the US. The recall was initiated on 28 Oct 2016 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-0223-2017
- FDA event ID
- 75537
- Recalling firm
- Love My Tru Body, McDonough, GA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Oct 2016
- FDA classified
- 22 Dec 2016
- Reported
- 28 Dec 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
Timeline
| 28 Oct 2016 | Recall initiated by company | |
| 22 Dec 2016 | Classified by FDA | +55 days |
| 28 Dec 2016 | 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: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.
Product as listed by the FDA
Skinny Bee Diet capsules, 500 mg, packaged in a 60-count bottle
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed without an approved NDA/ANDA: presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and phenolphthalein.
Which lots are affected?
Bottles stamped MFD: 03.07.2016 EXP: 03.06.2018
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.