CLASS I Drug recall · Reported 27 Dec 2017 · FDA Enforcement Report
LaBri's Body Health Atomic Exclusively distributed recalled
EZWeightLossTX is recalling LaBri's Body Health Atomic Exclusively distributed worldwide by LaBri's Body Health, distributed nationwide in the US. The recall was initiated on 24 Jul 2017 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-0121-2018
- FDA event ID
- 77817
- Recalling firm
- EZWeightLossTX, Corpus Christi, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 24 Jul 2017
- FDA classified
- 20 Dec 2017
- Reported
- 27 Dec 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
Timeline
| 24 Jul 2017 | Recall initiated by company | |
| 20 Dec 2017 | Classified by FDA | +149 days |
| 27 Dec 2017 | 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: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these 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
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Which lots are affected?
All lots remaining within expiry.
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
1 other product · FDA event 77817| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | LaBri's Body Health Xplode Exclusively distribute worldwide recalled | EZWeightLossTX | Hidden Drug Ingredients | Nationwide |
More recalls from EZWeightLossTX
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | LaBri's Body Health Xplode Exclusively distribute worldwide recalled | EZWeightLossTX | Hidden Drug Ingredients | Nationwide |