The Recall Desk
SevereFDA (Food)·H-0654-2026·Announced 2026-04-15

Blue Bull male enhancement supplement pouches contain undeclared sildenafil

Blue Bull Extreme Male Enhancement Supplement is being recalled after FDA analysis revealed the presence of undeclared sildenafil, a prescription drug ingredient not listed on the label.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: FDA Class I recall, which the rubric floors at Severe; no illnesses or deaths are reported in the source, so it does not escalate to Critical.

Plain-English summary

Blue Bull Extreme Male Enhancement Supplement, sold as boxes of 15 pouches at 15 g each, is being recalled by Pure Vitamins and Natural Supplements, LLC. The product carries UPC code 707443349917 and an expiry date of 02/2029.

FDA analysis revealed the presence of undeclared sildenafil. Sildenafil is the active ingredient in a prescription drug and is not declared on the product label. The FDA classified the action as Class I, its most serious classification.

The product was distributed in New Jersey. The quantity involved is not stated.

Consumers who have the product should stop using it. Anyone who has taken it and has health concerns, particularly people taking nitrate-containing medicines, should consult a healthcare professional.

The recalled product

Product
Blue 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
Manufacturer
Pure Vitamins and Natural Supplements, LLC
Category
Food — Dietary supplement
Hazard
  • undeclared-drug-ingredient
  • sildenafil
  • class-i
  • adulterated-supplement

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • EXP Date 02/2029

Distribution

Distribution scope not specified by the agency.

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