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Stop using now Food recall · FDA · Published March 13, 2026

Blue Bull Male Enhancement Supplement Recall: Undeclared Sildenafil Found

Pure Vitamins recalls 15 pouches of Blue Bull Extreme Male Enhancement Supplement due to undeclared sildenafil. Consumers should stop using if they have the product.

🇺🇸 FDA recall #H-0654-2026FoodBlue Bull ›
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Contact the company

Recalling firmPure Vitamins and Natural Supplements, LLC1708 E North Bay St · Tampa, FL 33610-7539
✎ GovInfoNow plain-language explainer

Pure Vitamins is recalling 15 pouches of Blue Bull Extreme Male Enhancement Supplement because FDA testing found undeclared sildenafil. This poses a risk of unintended medication effects since sildenafil is a prescription drug. Read more at govinfonow.com/recall/6652-blue-bull-male-enhancement-supplement-recall-undeclared-sildenafil-found.

Source Summary by GovInfoNow · govinfonow.com/recall/6652-blue-bull-male-enhancement-supplement-recall-undeclared-sildenafil-found · Updated August 10, 2026 · Official notice: FDA #H-0654-2026

Cite this page

“Blue Bull Male Enhancement Supplement Recall: Undeclared Sildenafil Found.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6652-blue-bull-male-enhancement-supplement-recall-undeclared-sildenafil-found. Based on FDA recall #H-0654-2026.

The FDA announced on March 13, 2026, that Pure Vitamins and Natural Supplements, LLC is recalling Blue Bull Extreme Male Enhancement Supplement due to undeclared sildenafil. The agency said the product poses a health risk because it contains an unapproved drug ingredient.

How to tell if you have it

  • Blue Bull Extreme Male Enhancement Supplement
  • UPC 707443349917
  • EXP Date 02/2029

The hazard

FDA analysis revealed the presence of undeclared sildenafil in the supplement. The product is classified as a Class I recall, indicating a high risk of adverse health consequences.

Context

GovInfoNow's records show Modern Warrior issued a dietary supplement recall for unapproved ingredients on Jan. 9, 2026. Sinus Cap herbal supplements were recalled on Nov. 20, 2025, due to unapproved drug claims on the label.

How to tell if you have this one

Check for the Blue Bull Extreme Male Enhancement Supplement with 15 pouches per box, each pouch weighing 15 grams. The product was made in the USA with an expiration date of February 2029 and UPC code 70744:3349917.

  • Brand
    Blue Bull
  • Product
    Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume
  • Category
    Food
FDA recall event · 3 products

All 3 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
    New Jersey
Recall numberProduct, codes & lots
H-0653-2026Boner Bears Honey Male Enhancement 100% Wildflower Honey, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume 1 entire pouch 30 minutes before Intercourse. MANUFACTURED IN: FLORIDA. UPC 788362191603; Lot # BBH0128 EXP 01/28
H-0654-2026Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Blue Bull Corporation Made In USA. UPC Code 707443349917; EXP Date 02/2029
H-0655-2026Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Entire Pouch 30 Minutes before Intercourse. Produced by Red Bull Corporation. Turkey www.redbullhoney.com UPC Code 9554100205595; B/N ORB524 MFG Date: MAY 2024 EXP DATE: MAY 2029
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the Blue Bull Extreme Male Enhancement Supplement if you have it.

Where it went and when

Where it was distributed

Distributed in New Jersey.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “New Jersey” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Jersey.

Recall timeline

FDA published this recall 33 days after the firm started it.

1. Firm started the recall: Mar 13, 202612. FDA classified it Class I: Apr 7, 202623. Published in FDA’s Enforcement Report: Apr 15, 202632026
  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 #H-0654-2026 (March 13, 2026)
  • Plain-language summary written by qwen3:4b on August 10, 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