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Unrated Drug recall · FDA · Published August 11, 2021

Hydro Pinapple Burn Max Health Thach Dua: Unapproved Sibutramine Risk

MATXI CORP's Hydro Pinapple Burn Max Health Thach Dua (20g x 10 sachets) contains undeclared sibutramine, a weight-loss drug not approved in the US. This recall covers all lots within expiry date.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0797-2021DrugMATXI CORP ›
Take action

Contact the company

Recalling firmEbay Seller - John Nguyen15710 Bryan Creek Ct · Houston, TX 77044-1437
✎ GovInfoNow plain-language explainer

MATXI CORP recalled their Hydro Pinapple Burn Max Health Thach Dua weight-loss product because it contains undeclared sibutramine, a drug not approved for use in the US. This poses a risk of serious health effects due to the unapproved ingredient. Read more at govinfonow.com/recall/35983-hydro-pinapple-burn-max-health-thach-dua-unapproved-sibutramine-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35983-hydro-pinapple-burn-max-health-thach-dua-unapproved-sibutramine-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0797-2021

Cite this page

“Hydro Pinapple Burn Max Health Thach Dua: Unapproved Sibutramine Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35983-hydro-pinapple-burn-max-health-thach-dua-unapproved-sibutramine-risk. Based on FDA recall #D-0797-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0797-2021%22&limit=1).

The FDA announced on August 11, 2021, that eBay seller John Nguyen is recalling Hydro Pinapple Burn Max Health Thach Dua by MATXI CORP due to the presence of undeclared sibutramine. The drug was marketed without an approved New Drug Application or Abbreviated New Drug Application.

How to tell if you have it

  • Hydro Pinapple Burn Max Health Thach Dua, packaged in a box containing 20g x 10 goi/sachets, MATXI CORP
  • UPC 8 936188 880108

The hazard

The product contains undeclared sibutramine and was marketed without an approved NDA or ANDA. The recall is classified as Class I, the most serious category.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21). OneSource Specialty Pharma Methohexital Sodium Recall occurred on 2026-06-07.

How to tell if you have this one

Check for the product name 'Hydro Pinapple Burn Max Health Thach Dua' in a box with 20g x 10 sachets. The product was sold by eBay seller John Nguyen and has the UPC 8 936188 880108. All lots within expiry date are included.

  • Brand
    MATXI CORP
  • Product
    Hydro Pinapple Burn Max Health Thach Dua, packaged in a box containing 20g x 10 goi/sachets, MATXI CORP, UPC 8 936188
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the product name and UPC code to confirm if it matches the recalled item.

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: “USA 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 2.2 years after the firm started it.

1. Firm started the recall: Aug 11, 202112. FDA classified it Class I: Sep 14, 202123. Published in FDA’s Enforcement Report: Sep 22, 202134. FDA terminated the recall: Oct 16, 2023420212023
  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-0797-2021 (August 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0797-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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