Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported December 27, 2017
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
EZWeightLossTX LLC recalled LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body … - a critical-severity action.
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body … was recalled by EZWeightLossTX LLC in December 27, 2017. Reason: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to b…. Check the official notice for the remedy. Verify recall #D-0121-2018 with the FDA Drug before acting.
The recall
EZWeightLossTX LLC issued this critical-severity FDA Drug recall-Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to b….
- Critical
- severity level
- Class I
- classification
- December 27, 2017
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0121-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0121-2018) was formally reported on December 27, 2017, with the manufacturer initiating the action on July 24, 2017. It is classified under Critical severity (Class I), with a current status of Terminated. EZWeightLossTX LLC is listed as the recalling firm, operating out of Corpus Christi, TX. Federal records list the affected scope as 4958 bottles.
The documented reason for this recall is: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplements: products found to be tainted with sibutramine making these unapproved drugs. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
4958 bottles
Related Recalls
6
0 from same agency
Product description
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0121-2018 |
| Date reported | December 27, 2017 |
| Date initiated | July 24, 2017 |
| Recalling firm | EZWeightLossTX LLC |
| Firm location | Corpus Christi, TX |
| Affected scope | 4958 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0121-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by LaBri's Body Health.. Recalled by EZWeightLossTX LLC. Units affected: 4958 bottles.
Why was this product 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 agency issued this recall? ▼
This recall was issued by the FDA Drug on December 27, 2017. Severity: Critical. Recall number: D-0121-2018.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0121-2018) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for t…
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported December 27, 2017. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.