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Stop using now Drug recall · FDA · Published April 14, 2025

Electro Buzz Dietary Supplement Recall: Unapproved Ingredients Found

Saini Trade Inc recalls Electro Buzz dietary supplements due to undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil found in lab tests. Consumers should stop using affected products.

🇺🇸 FDA recall #D-0465-2025DrugSaini Trade ›
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Recalling firmSAINI TRADE INC1405 N Scottsdale Rd · Tempe, AZ 85288-1714
✎ GovInfoNow plain-language explainer

Saini Trade Inc has recalled Electro Buzz dietary supplements after lab tests found undeclared drugs including chloropretadalafil, propoxyphenylsildenafil, and sildenafil. These substances are not approved for use in dietary supplements and could pose health risks. Read more at govinfonow.com/recall/32144-electro-buzz-dietary-supplement-recall-unapproved-ingredients-found.

Source Summary by GovInfoNow · govinfonow.com/recall/32144-electro-buzz-dietary-supplement-recall-unapproved-ingredients-found · Updated August 17, 2026 · FDA enforcement record: FDA #D-0465-2025

Cite this page

“Electro Buzz Dietary Supplement Recall: Unapproved Ingredients Found.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32144-electro-buzz-dietary-supplement-recall-unapproved-ingredients-found. Based on FDA recall #D-0465-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0465-2025%22&limit=1).

SAINI TRADE INC recalled ELECTRO BUZZ dietary supplement nationwide on April 14, 2025, according to the FDA. The product is tainted with undeclared drugs and poses a Class I hazard.

How to tell if you have it

  • Brand: Saini Trade
  • Product: ELECTRO BUZZ, Dietary Supplement, 10 capsules per box
  • Distributed By: Health Fixer, Tempe, AZ 85288
  • UPC: B0DK68LF6J
  • Lot #: KT-1ST-43-01-07/2024, Exp. 10/15/2026

The hazard

Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar products include Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21), StuffbyNainax MR 7 SUPER 700000 Capsules: FDA Finds Undeclared Sildenafil and Tadalafil (2025-12-15), and Shoolin Pharma Chem Sildenafil Recall (2026-08-03).

How to tell if you have this one

Check for the UPC B0DK68LF6J and lot number KT-1ST-43-01-07/2024 on the product packaging. The product was distributed by Health Fixer in Tempe, AZ.

  • Brand
    Saini Trade
  • Category
    Drug
FDA recall event · 5 products

All 5 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
    Ongoing
  • Distribution
    Nationwide
Recall numberProduct, codes & lotsQuantity
D-0463-2025Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.; All Lots Lot #: KT-1ST-43-01-10-2025, Exp. 01/10/20273000 boxes
D-0464-2025MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.; All lots Lot #: KT-1ST-43-01-04/2026, Exp. 04/25/2026500 boxes
D-0465-2025ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.; All lots Lot #: KT-1ST-43-01-07/2024, Exp. 10/15/2026300 boxes
D-0466-2025ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.; All lots Lot #: KT-1ST-43-01-10/2025, Exp. 01/10/2027500 boxes
D-0467-2025Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.; All lots Lot #: KT-1ST-43-0110/2025, Exp. 03/15/2026300 boxes
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using Electro Buzz dietary supplements with the UPC B0DK68LF6J and lot number KT-1ST-43-01-07/2024.

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 published this recall 2 months after the firm started it.

1. Firm started the recall: Apr 14, 202512. FDA classified it Class I: Jun 11, 202523. Published in FDA’s Enforcement Report: Jun 18, 202532025
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

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-0465-2025 (April 14, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0465-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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