SlimeX-15 Capsule Recall: Undeclared Sibutramine Hazard
Bee Extremely Amazed LLC recalls SlimeX-15 Capsules due to undeclared sibutramine, an unapproved appetite suppressant withdrawn for safety reasons.
Stop using this now
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
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What happened, in plain English
Bee Extremely Amazed LLC is recalling SlimeX-15 Capsules (15 mg, 30-count bottles) because the product contains undeclared sibutramine. Sibutramine is an appetite suppressant that was removed from the U.S. market due to safety concerns, making this product an unapproved drug rather than a safe dietary supplement. The recall covers all lots of this product distributed nationwide. Read more at govinfonow.com/recall/43325-slimex-15-capsule-recall-undeclared-sibutramine-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/43325-slimex-15-capsule-recall-undeclared-sibutramine-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #D-1146-2016
Cite this page
“SlimeX-15 Capsule Recall: Undeclared Sibutramine Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43325-slimex-15-capsule-recall-undeclared-sibutramine-hazard. Based on FDA recall #D-1146-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1146-2016%22&limit=1).
Why it’s dangerous
The capsules contain sibutramine, an ingredient that was withdrawn from the U.S. market for safety reasons. Because this ingredient is undeclared and unapproved, users cannot know they are consuming a potentially dangerous substance when taking the supplement.
Who’s affected
Consumers who purchased SlimeX-15 Capsules marketed by Signature Pharmaceuticals Ltd. are affected. Individuals seeking weight loss or appetite suppression are at risk of ingesting a withdrawn, unsafe drug ingredient.
How to tell if you have this one
Look for SlimeX-15 Capsules in 30-count bottles containing 15 mg of product. The item is marketed by Signature Pharmaceuticals Ltd. (Mumbai) and manufactured in India by HAB Pharmaceuticals & Research Limited. All lots are included in this recall.
- Brand
SlimeX- Category
Drug
All 14 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-1138-2016 | Asset BOLD Capsules, 500 mg, 60-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com; All lots | N/A |
| D-1139-2016 | Asset extreme+PLUS Capsules, 500 mg, 30-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com www.allnaturalbeelievers.com; All lots | N/A |
| D-1140-2016 | EVOLVE BEE POLLEN Capsules, 250mg, 60-count bottles, Manufactured for 2637 E. Atlantic Blvd, Pompano Beach, Florida, 33062 WWW.BEEEXTREMELYAMAZED.COM; All lots | N/A |
| D-1141-2016 | Infinity Capsules, 500 mg, 30-count bottle, Manufactured for Floyd Nutrition; All lots | N/A |
| D-1142-2016 | Jenesis Capsules, 350 mg, 60-count bottles, Manufactured for Timeless Solutions 1810 E. Sahara Ave #100 Las Vegas, Nevada 89104; All lots | 79 bottles |
| D-1143-2016 | La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando, FL 32801 (407) 930-4043; All lots | N/A |
| D-1144-2016 | Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando FL 32801 (407)930-4043; All lots | 581 bottles |
| D-1145-2016 | Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203; All lots | 1,104 bottles |
| D-1146-2016 | SlimeX-15 Capsules, 15 mg, 30-count bottles, Marketed by: Signature Pharmaceuticals Ltd. MUMBAI-400-030 Manufactured in India by: HAB Pharmaceuticals & Research Limited 10-Pharma City, SIDCUL, Selaqui, Dehradun, 248 197; All lots | N/A |
| D-1147-2016 | SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition; All lots | N/A |
| D-1148-2016 | Ultimate Formula Capsules, 250mg, 48-count bottles, Manufactured for: Zi Xiu Tang Success, LLC Trexlertown, PA 18087, USA www.zixiutangsuccess.com; All lots | N/A |
| D-1149-2016 | XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health; All lots | N/A |
| D-1150-2016 | XCEL ADVANCED Capsules, 350mg, 60-count bottles, Manufactured for JNS Health; All lots | N/A |
| D-1151-2016 | ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles; All lots | N/A |
What to do — step by step
Stop using the capsules
Do not consume any remaining SlimeX-15 Capsules due to the presence of undeclared sibutramine.
Discard or return the product
The recall record does not specify a specific remedy such as a refund or return address; consumers should dispose of the product safely.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 4.4 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-1146-2016 (December 15, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1146-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.