- Recall Issued: April 25, 2025
- Announced By: FDA on April 29, 2025
- Company: Health Fixer
- Product Name: Male Ultra, Malextra, Electro Buzz, Ultra Armor, Male Ultra Pro
- Reason: Presence of undeclared pharmaceutical ingredients (Chloropretadalafil, Propoxyphenylsildenafil, Sildenafil)
- Issue: These undeclared ingredients are analogues of drugs used to treat erectile dysfunction and pose serious health risks
- Product Details: Sold in 10-capsule blister packs, nationwide via Amazon
- Action Required: Stop use immediately, discard products, consult a doctor if any symptoms arise
Wanna know more about what happened? Read more below!
What happened?
On April 25, 2025, Health Fixer announced a voluntary nationwide recall of five of its male enhancement supplements after laboratory tests detected undeclared pharmaceutical compounds in the products. These unapproved ingredients—sildenafil, chloropretadalafil, and propoxyphenylsildenafil—mimic prescription drugs used to treat erectile dysfunction and can be dangerous when used without medical supervision.
The company discovered the issue after third-party lab testing and, as of now, no adverse events have been reported. However, due to the potential for severe health complications, especially in men taking heart medications, this recall is being taken seriously.
Recalled products table
Brand | Product | Size | UPC/NDC | Best By Date | Issue |
Health Fixer | Male Ultra | 10-capsule blister | B0CMQ4FTHG | 01/10/2027 | Undeclared sildenafil & analogues |
Health Fixer | Malextra | 10-capsule blister | B0CWKZ6ZP3 | 04/25/2026 | Same |
Health Fixer | Electro Buzz | 10-capsule blister | B0DK68LF6J | 10/15/2026 | Same |
Health Fixer | Ultra Armor | 10-capsule blister | B0CYJ7Y5H9 | 01/10/2027 | Same |
Health Fixer | Male Ultra Pro | 10-capsule blister | B0CZN7C6YH | 03/15/2026 | Same |
What caused the issue?
The root of the recall lies in undeclared pharmaceutical ingredients found in Health Fixer’s line of male enhancement supplements. These aren’t just any extra herbs or vitamins—they’re powerful drug compounds, typically found in prescription-only medications for erectile dysfunction.
What’s in these supplements?
- Sildenafil – The active ingredient in Viagra, a PDE-5 inhibitor.
- Chloropretadalafil & Propoxyphenylsildenafil – Chemical analogues of sildenafil, structurally similar and believed to have comparable effects and risks.
None of these ingredients were listed on the product labels, which is a big no-no in FDA land. Why? Because it means consumers are unknowingly ingesting drugs that can interact dangerously with other medications.
Why this is a big deal
When taken without medical supervision, these ingredients can:
- Cause life-threatening drops in blood pressure when combined with nitrates (commonly prescribed for chest pain and heart issues)
- Lead to severe interactions for people with conditions like:
- Diabetes
- Hypertension (high blood pressure)
- Heart disease
- High cholesterol
- Mask symptoms or interfere with treatments for serious conditions
Who’s at risk?
- Adult males taking heart medications (especially nitrates)
- Older adults with pre-existing health issues
- Anyone unaware they’re ingesting potent, unapproved drugs
Potential symptoms
If someone unknowingly takes these supplements, they may experience:
- Sudden, extreme drop in blood pressure
- Dizziness or fainting
- Chest pain
- Irregular heartbeat
- Severe headaches
- Visual disturbances
- Flushing and heart palpitations
- In extreme cases: stroke or heart attack
10 common questions you might have
1. What’s actually in these supplements that caused the recall?
They contain sildenafil and two similar compounds not listed on the label, all of which are used to treat erectile dysfunction.
2. Why is this dangerous if I’m already healthy?
Even if you’re healthy, mixing these drugs with other medications—or taking them without guidance—can trigger unexpected and serious side effects.
3. Are these drugs illegal?
Not exactly. Sildenafil is legal when prescribed, but it’s illegal to sell it in a supplement without FDA approval or labeling it properly.
4. Can I keep using the product if I haven’t had issues?
Nope. Stop immediately. Just because you haven’t felt anything doesn’t mean it’s safe. The risks are cumulative and unpredictable.
5. How do I know if I have one of the recalled lots?
Check the UPC and expiration date on the blister pack. Refer to the table above for specific codes and dates.
6. I bought this on Amazon—how did this happen?
Amazon is a major reseller, and unfortunately, not all third-party products undergo thorough vetting. That’s why transparency and testing are critical.
7. Is it OK to just toss it in the trash?
You should dispose of it safely, ideally via a local medication drop-off site, or follow FDA disposal guidelines. When in doubt, contact your local pharmacy.
8. Can I get a refund?
The company hasn’t listed a refund policy, but you can reach out to Health Fixer directly via phone or email (see contact details above).
9. Have other brands been recalled for this reason?
Yes—there’s been a string of similar recalls. Check out recent PDE-5 supplement recalls here.
10. What should I do if I feel symptoms?
Contact a healthcare provider right away. And consider reporting your experience through the FDA’s MedWatch program.
Here’s what you should do
- Stop Using Immediately: These aren’t your average over-the-counter vitamins
- Check the Label: Look for the UPC codes and expiration dates listed above
- Contact Health Fixer:
- Phone: 414-888-8818
- Email: [email protected] (Mon–Fri, 9am–6pm MT)
- Talk to Your Doctor: If you’ve taken these supplements, better safe than sorry
- Report Issues to the FDA:
Behind the brand
Health Fixer, based in Tempe, AZ, markets various wellness products—mostly in the form of dietary supplements sold online. While this is a first-time recall for the brand, similar issues have plagued the supplement industry.
Déjà Vu? You’re not wrong. Here are other recent recalls with similar causes:
- On April 14, 2025, Supplement Manufacturing Partners, Inc. issued a voluntary recall of its Dorado Nutrition brand Spermidine Maximum Strength 10mg Vegetable Capsules due to—brace yourself—undeclared wheat.
- On December 16, 2025, GNMART Inc. issued a nationwide voluntary recall of its Force Forever Joint Pain Supplement due to the presence of undeclared drug ingredients, Diclofenac and Dexamethasone.
“Recalls like this one are a wake-up call for the supplement industry. Transparency isn’t optional—it’s the bedrock of consumer safety and trust. When companies fail to disclose potent pharmaceutical ingredients, especially in products targeting vulnerable consumers, it puts lives at risk. It’s not just about following the rules; it’s about taking real responsibility through rigorous testing and proactive quality controls. This situation underscores the need for brands to treat safety as a core value, not an afterthought. As an industry, we have a duty to raise the bar and protect the people who rely on our products.” — Eran Mizrahi, CEO of Source86
Ensuring safe eats
This recall serves as another wake-up call for the supplement industry. Mislabeling or undisclosed pharmaceutical ingredients can have serious health consequences, especially for individuals already managing medical conditions.
Manufacturers and private label brands need to:
- Vet their suppliers rigorously
- Conduct independent lab testing
- Stay FDA-compliant with labeling and formulation
If you’re sourcing supplements or ingredients for a co-packing, private label, or manufacturing operation, it’s crucial to know exactly what’s going into your product.Have questions about safe ingredient sourcing? Our team is here to help. For more insights, feel free to contact us or explore our range of high-quality, tested ingredients. Let’s chat!
