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Stop using now Drug recall · FDA · Published December 9, 2015

Lucy's Weight Loss Pink Bikini Capsule Recall: Undeclared Drugs

Lucy's Weight Loss recalls all Pink Bikini capsules due to undeclared Sibutramine, Phenolphthalein, and/or Diclofenac. Check your bottle.

🇺🇸 FDA recall #D-0882-2016DrugLucy's Weight Loss ›
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Contact the company

Recalling firmLucy's Weight Loss (dba. Waisted With Lucy)813 Oram St · Arlington, TX 76010-2837
✎ GovInfoNow plain-language explainer

What happened, in plain English

Lucy's Weight Loss (dba Waisted With Lucy) is recalling all lots of Pink Bikini capsules in 30-count bottles because they contain undeclared prescription drugs. The product was marketed without an approved New Drug Application or Abbreviated New Drug Application. These undeclared ingredients pose serious health risks that are not disclosed on the label. Read more at govinfonow.com/recall/43343-lucy-s-weight-loss-pink-bikini-capsule-recall-undeclared-drugs.

Source Summary by GovInfoNow · govinfonow.com/recall/43343-lucy-s-weight-loss-pink-bikini-capsule-recall-undeclared-drugs · Updated October 11, 2026 · FDA enforcement record: FDA #D-0882-2016

Cite this page

“Lucy's Weight Loss Pink Bikini Capsule Recall: Undeclared Drugs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/43343-lucy-s-weight-loss-pink-bikini-capsule-recall-undeclared-drugs. Based on FDA recall #D-0882-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0882-2016%22&limit=1).

Why it’s dangerous

The capsules contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac. These ingredients are prescription drugs that can cause serious side effects, including heart problems, high blood pressure, liver damage, or gastrointestinal bleeding, without the consumer's knowledge or proper medical supervision.

Who’s affected

Consumers who purchased Pink Bikini capsules from nationwide distribution channels between any dates prior to the recall notice. Individuals using weight loss supplements are at risk of ingesting undeclared pharmaceutical substances.

How to tell if you have this one

Look for Pink Bikini capsules in any color and strength, packaged in a 30-count bottle. The product was manufactured and distributed by Lucy's Weight Loss System (dba Waisted With Lucy) of Arlington, TX 76010. All lots are included in this recall.

  • Brand
    Lucy's Weight Loss
  • Category
    Drug
FDA recall event · 2 products

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 numberProduct, codes & lots
D-0882-2016Pink Bikini capsules, (all colors and all strengths), packaged in 30-count bottle, Manufactured and Distributed by: Lucy's Weight Loss System (dba Waisted With Lucy), Arlington, TX 76010; All lots, all colors and all strengths
D-0883-2016Shorts on the Beach capsules, (all colors and all strengths), packaged in 30-count bottle, Manufactured and Distributed by: Lucy's Weight Loss System (dba Waisted With Lucy), Arlington, TX 76010; All lots, all colors and all strengths
Based on the official FDA remedy

What to do — step by step

  1. Stop taking the capsules

    Discontinue use immediately due to the presence of undeclared drugs that may cause serious health issues.

  2. Discard or return product

    The recall record does not specify a specific remedy such as a refund or return address, so consumers should dispose of the product safely or contact the distributor for 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 5.8 years after the firm started it.

1. Firm started the recall: Dec 9, 201512. FDA classified it Class I: May 26, 201623. Published in FDA’s Enforcement Report: Jun 1, 201634. FDA terminated the recall: Sep 27, 2021420152021
  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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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-0882-2016 (December 9, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0882-2016 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.
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