EZWeightLossTX LLC recalls LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
LaBri's Body Health recalls Atomic 60 Capsules due to being marketed as dietary supplements but containing unapproved drug sibutramine. Consumers should stop using these products immediately.
Stop using this now
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Contact the company & request your remedy
What happened, in plain English
LaBri's Body Health is recalling its Atomic 60 Capsules because they contain unapproved drug sibutramine and were marketed as dietary supplements. This poses a risk of serious health effects since sibutramine is a controlled substance. Read more at govinfonow.com/recall/41429-lab-body-health-atomic-60-capsules-recall-unapproved-drug-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/41429-lab-body-health-atomic-60-capsules-recall-unapproved-drug-risk · Updated October 7, 2026 · FDA enforcement record: FDA #D-0121-2018
Cite this page
“LaB: Body Health Atomic 60 Capsules Recall: Unapproved Drug Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/41429-lab-body-health-atomic-60-capsules-recall-unapproved-drug-risk. Based on FDA recall #D-0121-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0121-2018%22&limit=1).
Why it’s dangerous
These capsules contain sibutramine, a drug that was banned in many countries and is known to cause serious health issues like heart problems and psychiatric symptoms. The product was marketed as a dietary supplement but is actually an unapproved drug.
Who’s affected
Anyone who purchased LaBri's Body Health Atomic 60 Capsules worldwide. People using these capsules for weight loss are at risk due to the unapproved drug content.
How to tell if you have this one
Check for LaBri's Body Health Atomic 60 Capsules. The product was distributed worldwide and all lots within their expiration date are affected.
- Brand
LaBri's Body Health- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0121-2018 | LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.; All lots remaining within expiry. | 4958 bottles |
| D-0122-2018 | LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by LaBri's Body Health.; All lots remaining within expiry. | 1424 bottles |
What to do — step by step
Stop Using Now
Immediately stop using LaBri's Body Health Atomic 60 Capsules as they contain unapproved drug sibutramine.
Questions people ask
Why are these capsules being recalled?
These capsules contain unapproved drug sibutramine and were marketed as dietary supplements, which is illegal.
What should I do if I have these capsules?
Stop using them immediately and contact LaBri's Body Health for further instructions.
Are there any safety risks from using these capsules?
Yes, sibutramine can cause serious health issues including heart problems and psychiatric symptoms.
Contact LaBri's Body Health
We’ve drafted a message you can send LaBri's Body Health to request your refund or repair — edit it as you like.
Subject: Recall D-0121-2018 — LaBri's Body Health LaBri's Body Health Hello, I own a LaBri's Body Health that is covered by recall D-0121-2018 from LaBri's Body Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0121-2018 (July 24, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0121-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.