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Drug recall · FDA · Published February 14, 2018

Bella All Natural recalls Bella Capsules, 600mg, 30-count bottles, Manufactured for: Bella All Natural 304 E 11th Street, Los Angeles, CA 90015

Bella All Natural recalls 600mg capsules due to undeclared sibutramine, a withdrawn controlled substance. Safety risks not established for this unapproved drug.

🇺🇸 FDA recall #D-0593-2018DrugBella All Natural ›
Take action

Contact the company & request your remedy

Recalling firmBella All Natural304 E 11th St, N/A · Los Angeles, CA 90015-1715
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bella All Natural is recalling 600mg capsules because they contain sibutramine, a drug previously approved but withdrawn from the U.S. market in 2010 due to safety concerns. This product is unapproved and has not been tested for safety or effectiveness. Read more at govinfonow.com/recall/40812-bella-capsules-600mg-recall-unapproved-drug-contains-sibutramine.

Source Summary by GovInfoNow · govinfonow.com/recall/40812-bella-capsules-600mg-recall-unapproved-drug-contains-sibutramine · Updated October 7, 2026 · FDA enforcement record: FDA #D-0593-2018

Cite this page

“Bella Capsules 600mg Recall: Unapproved Drug Contains Sibutramine.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/40812-bella-capsules-600mg-recall-unapproved-drug-contains-sibutramine. Based on FDA recall #D-0593-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0593-2018%22&limit=1).

Why it’s dangerous

The capsules contain sibutramine, a controlled substance withdrawn from the U.S. market in 2010 because of safety concerns. Since this product is unapproved and not tested for safety, it could pose health risks that haven't been established.

Who’s affected

People who own or use Bella All Natural 600mg capsules manufactured on or after October 15, 2017, are affected. Those with medical conditions or taking other medications may be at higher risk.

How to tell if you have this one

Check for 600mg capsules with the lot number MFD:10.15.2017, Exp.10/14/2019. The product was manufactured for Bella All Natural at 304 E 11th Street in Los Angeles, CA.

  • Brand
    Bella All Natural
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number MFD:10.15.2017, Exp.10/14/2019 on the bottle.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The product contains sibutramine, a controlled substance withdrawn from the U.S. market in 2010 due to safety concerns. This makes it an unapproved drug with unestablished safety and effectiveness.

Is there a remedy for this product?

The recall record does not specify a remedy.

What is the risk of using this product?

The product is unapproved and has not been tested for safety, so potential health risks are unknown.

Take action

Contact Bella All Natural

We’ve drafted a message you can send Bella All Natural to request your refund or repair — edit it as you like.

Subject: Recall D-0593-2018 — Bella All Natural Bella All Natural

Hello,

I own a Bella All Natural that is covered by recall D-0593-2018 from Bella All Natural.

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-0593-2018 (February 14, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0593-2018 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA