Blue Bull Extreme Male Enhancement Supplement recall (April 2026): reason, lots, what to do
Not medical advice. This page reproduces one FDA enforcement report and explains its fields; FDA’s text is quoted as FDA’s. If you have this product and any symptoms, your pharmacist or doctor comes before this page.
What was recalled
Pure Vitamins and Natural Supplements, LLC (Tampa, FL) recalled Blue Bull Extreme Male Enhancement Supplement and 1 other product in a recall FDA classified as Class I. FDA’s stated reason: “FDA analysis revealed the presence of undeclared sildenafil”. Started March 13, 2026; posted in the enforcement report April 15, 2026; status Ongoing.
Class I means, in FDA’s words, a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Distribution: “New Jersey”. Quantity: Unknown; Unknown. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 98592, retrieved from openFDA on September 21, 2026; the last row links to the live record so you can confirm it has not changed.
| Recalling firm | Pure Vitamins and Natural Supplements, LLC, Tampa, FL |
|---|---|
| Products | Red 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 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 |
| Reason for recall (FDA’s text) | “FDA analysis revealed the presence of undeclared sildenafil” |
| Classification | Class I |
| Status | Ongoing |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2026-03-13 |
| Enforcement report date | 2026-04-15 |
| FDA classified on | 2026-04-07 |
| Distribution | New Jersey |
| Quantity | Unknown; Unknown |
| How the firm notified | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Recall numbers | H-0655-2026, H-0654-2026 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
B/N ORB524 MFG Date: MAY 2024 EXP DATE: MAY 2029EXP Date 02/2029
Find the lot number on the bottom of the container, beside the seal or on the box flap; the expiration date is usually printed next to it. If the code on your container appears above, it is in scope. If the product name matches but the code does not, your unit is not part of this recall, though a second lot is sometimes added later, so re-check the recall list before finishing the bottle.
Why this is a Class I recall
FDA assigns the class by the probability and severity of harm, not by how much product is involved. For this event the reason falls into what we file as hidden drug or prohibited ingredient: a substance that is not a lawful dietary ingredient was found in, or substituted for, the product. This is the recall category with the least warning for the buyer: the label reads like a supplement and the effect comes from something else.
FDA’s definition of Class I (21 CFR 7.3) is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. A Class I recall is the strongest signal FDA sends about a consumer product short of a seizure; it is reserved for the cases where continuing to use the product is itself the risk. The reason text is the authority for this specific event; the class is FDA’s summary judgement of it.
If you bought it
- Stop taking it now; for a Class I recall this is the point of the notice.
- Match your lot against the codes above. Keep the container: the firm’s notice normally offers a refund on proof of the lot number or a photo.
- If you take prescription medicines, tell your pharmacist which product you were taking; an undeclared ingredient can interact with what you are prescribed. Then report to FDA MedWatch (online form or 1-800-FDA-1088).
- Check the firm’s other products. This event already covers 2 products. Search “Pure Vitamins and Natural Supplements, LLC” on the full recall list.
Choosing a replacement that can be checked
This product does not name an ingredient we track, so there is no like-for-like guide to send you to. The general rule holds: the only supplements whose contents a buyer can verify are those in a certifier’s public registry (NSF/ANSI 173, NSF Certified for Sport, USP Verified, Informed Sport) or with a lot-specific certificate of analysis the brand publishes. Our registry audit shows how few products clear that bar, and the per-ingredient third-party-tested pages (magnesium, creatine, vitamin D, omega-3, multivitamins) list the ones that do.
Frequently asked questions
Why was Blue Bull Extreme Male Enhancement Supplement recalled?
FDA's enforcement report gives the reason as: "FDA analysis revealed the presence of undeclared sildenafil". FDA records the recall type as "Voluntary: Firm initiated"; Pure Vitamins and Natural Supplements, LLC of Tampa, FL started it March 13, 2026 and it was posted in FDA's enforcement report on April 15, 2026 as Class I.
Which lots of Blue Bull Extreme Male Enhancement Supplement are affected?
FDA's record lists: B/N ORB524 MFG Date: MAY 2024 EXP DATE: MAY 2029 | EXP Date 02/2029. Match these against the lot number, UPC or expiration date printed on your container; a bottle whose code is not listed is not part of this recall.
Where was Blue Bull Extreme Male Enhancement Supplement sold?
FDA's record gives the distribution as: "New Jersey". Quantity recalled: Unknown; Unknown.
Is this recall over?
FDA lists the status as "Ongoing". Ongoing means the firm is still retrieving product from the market.
← Every FDA dietary supplement recall since 2023 · How we score supplement safety
Sources
- U.S. Food and Drug Administration. Enforcement report, event 98592, recall numbers H-0655-2026, H-0654-2026. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-0655-2026 · H-0654-2026
- 21 CFR 7.3(m): recall classification definitions. eCFR Title 21 Part 7.
- FDA. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. fda.gov/safety/medwatch.