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Stop using now Drug recall · FDA · Published October 28, 2016

Love My Tru Body Recalls Skinny Bee Diet Capsules Due to Undeclared Drugs

Love My Tru Body recalls 74 bottles of Skinny Bee Diet capsules nationwide due to undeclared sibutramine and phenolphthalein. Check your bottle.

🇺🇸 FDA recall #D-0223-2017DrugLove My Tru Body ›
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Recalling firmLove My Tru Body289 Jonesboro Rd Ste 106 · McDonough, GA 30253-3725
✎ GovInfoNow plain-language explainer

What happened, in plain English

Love My Tru Body is recalling Skinny Bee Diet capsules (500 mg) because they contain undeclared prescription drugs sibutramine and desmethylsibutramine, as well as the laxative phenolphthalein. These ingredients are not listed on the label and pose serious health risks. The recall affects 74 bottles distributed nationwide. Read more at govinfonow.com/recall/42270-love-my-tru-body-recalls-skinny-bee-diet-capsules-due.

Source Summary by GovInfoNow · govinfonow.com/recall/42270-love-my-tru-body-recalls-skinny-bee-diet-capsules-due · Updated October 11, 2026 · FDA enforcement record: FDA #D-0223-2017

Cite this page

“Love My Tru Body Recalls Skinny Bee Diet Capsules Due to Undeclared Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/42270-love-my-tru-body-recalls-skinny-bee-diet-capsules-due. Based on FDA recall #D-0223-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0223-2017%22&limit=1).

Why it’s dangerous

The product contains sibutramine, a drug withdrawn from the market due to cardiovascular risks, and its metabolite desmethylsibutramine. It also contains phenolphthalein, a laxative that has been banned for over-the-counter use due to potential carcinogenicity.

Who’s affected

Consumers who purchased Skinny Bee Diet capsules, specifically those with bottles stamped MFD: 03.07.2016 and EXP: 03.06.2018, are at risk of ingesting undeclared pharmaceutical ingredients.

How to tell if you have this one

Look for Skinny Bee Diet capsules in a 60-count bottle. Check the bottom of the bottle for the stamped manufacturing date (MFD: 03.07.2016) and expiration date (EXP: 03.06.2018).

  • Brand
    Love My Tru Body
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop taking the capsules immediately

    Do not consume any more of the product due to the presence of undeclared drugs.

  2. Discard or return the product

    The record does not specify a return address or refund process; contact the manufacturer for further instructions.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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 5 months after the firm started it.

1. Firm started the recall: Oct 28, 201612. FDA classified it Class I: Dec 22, 201623. Published in FDA’s Enforcement Report: Dec 28, 201634. FDA terminated the recall: Apr 6, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Questions people ask

Where were these products sold?

The recall distribution pattern is listed as nationwide.

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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-0223-2017 (October 28, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0223-2017 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.
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