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Unrated Drug recall · FDA · Published March 19, 2024

Pyramids Wholesale Recalls Weiner Boner Honey Due to Undeclared Sildenafil

Pyramids Wholesale recalls 100% Organic Weiner Boner Honey packets for containing undeclared sildenafil and tadalafil without FDA approval.

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

🇺🇸 FDA recall #D-0449-2024DrugPyramids Wholesale ›
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Contact the company

Recalling firmPyramids Wholesale Inc.464 E 4th St · Los Angeles, CA 90013-1604
✎ GovInfoNow plain-language explainer

Pyramids Wholesale is recalling their 100% Organic Weiner Boner Honey packets because they contain undeclared sildenafil and tadalafil without FDA approval. This poses a risk of serious health effects due to unapproved drug ingredients. Read more at govinfonow.com/recall/32767-pyramids-wholesale-recalls-weiner-boner-honey-due-to-undeclared-sildenafil.

Source Summary by GovInfoNow · govinfonow.com/recall/32767-pyramids-wholesale-recalls-weiner-boner-honey-due-to-undeclared-sildenafil · Updated August 18, 2026 · FDA enforcement record: FDA #D-0449-2024

Cite this page

“Pyramids Wholesale Recalls Weiner Boner Honey Due to Undeclared Sildenafil.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/32767-pyramids-wholesale-recalls-weiner-boner-honey-due-to-undeclared-sildenafil. Based on FDA recall #D-0449-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0449-2024%22&limit=1).

Pyramids Wholesale Inc. is voluntarily recalling Weiner Boner Honey, a 12g packet marketed as an organic formula, after the FDA found it contained undeclared sildenafil and/or tadalafil. The Food and Drug Administration announced the Class I recall on March 19, 2024.

How to tell if you have it

  • Brand: Pyramids Wholesale
  • Product: Weiner Boner Honey, 12g packet, 100% Organic Formula
  • All lots
  • Quantity: 19 boxes
  • Distribution: Nationwide in the USA

The hazard

The products were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). They were found to contain undeclared sildenafil and/or tadalafil.

Context

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

How to tell if you have this one

The product is labeled 'Weiner Boner Honey, 12g packet, 100% Organic Formula.' All lots are affected, so no specific lot numbers are needed.

  • Brand
    Pyramids Wholesale
  • Category
    Drug
FDA recall event · 11 products

All 11 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 in the USA
Recall numberProduct, codes & lotsQuantity
D-0448-2024Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455; All lots45 boxes
D-0449-2024Weiner Boner Honey, 12g packet, 100% Organic Formula.; All lots19 boxes
D-0450-2024Flower Power, CBD infused Female Enhancement, 59 ml bottle, UPC 0 678741 351646.; All lotsN/A
D-0451-2024Samurai-X Honey 6800, UPC 2 56891 27553 3.; All lotsN/A
D-0452-2024Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557; All Lots149 boxes
D-0453-2024GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.; All lots12 boxes
D-0454-2024libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.; All lots7 boxes
D-0455-2024SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl. oz., UPC 8 700470 032762; All lots7 pieces
D-0456-2024The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack, Distributed by Hombres LLC, 130 Maccormick Ave, Suite 105, Costa Mesa, A, UPC 6 61631 26363 1.; All lots10 boxes
D-0457-2024ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'L; All lots4,351 pieces
D-0458-2024HONEY MANUKA BUNNY LOVE, 12g, All Natural Sexual Enhancement, UPC: N/A; All lots19 boxes
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name 'Weiner Boner Honey, 12g packet, 100% Organic Formula' on the label.

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 in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 43 days after the firm started it.

1. Firm started the recall: Mar 19, 202412. FDA classified it Class I: Apr 22, 202423. Published in FDA’s Enforcement Report: May 1, 202432024
  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-0449-2024 (March 19, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0449-2024 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