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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

VitalityXtra, PeakMax, ZoomMax, and ZapMax Recalled for Undeclared Drugs

Agency Publication Date: December 2, 2024
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Summary

Boulla LLC is recalling several capsule products marketed as dietary supplements, including VitalityXtra, PeakMax, ZoomMax, and ZapMax, because they were found to contain undeclared sildenafil and diclofenac. Sildenafil is an active ingredient in prescription drugs used for erectile dysfunction, and diclofenac is a non-steroidal anti-inflammatory drug (NSAID). These pharmaceutical ingredients are not listed on the product labels and were distributed nationwide in 10-count blister packs.

Risk

Undeclared sildenafil can interact with nitrates in prescription drugs (like those used for heart conditions), potentially lowering blood pressure to life-threatening levels. Undeclared diclofenac increases the risk of serious cardiovascular events, such as heart attack or stroke, and can cause severe gastrointestinal damage, including bleeding and ulceration.

What You Should Do

  1. This recall affects VitalityXtra and PeakMax (lot 230811, expiration date 08/11/2025) as well as ZoomMax and ZapMax (lot YZM240406, expiration date 04/05/2027). All affected products are 500 mg capsules sold in 10-count blister packs.
  2. If you have health concerns, contact your healthcare provider or pharmacist.
  3. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional information regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: VitalityXtra Capsules (500 mg)by VitalityXtra
Variants: 500 mg, 10 count blister
Lot Numbers:
230811 (Exp: 08/11/2025)

Distributed by: VitalityXtra, San Francisco, CA

Product: PeakMax Capsules (500 mg)by PeakMax
Variants: 500 mg, 10 count blister
Lot Numbers:
230811 (Exp: 08/11/2025)

Distributed by: PeakMax, San Francisco, CA

Product: ZoomMax Capsules (500 mg)by ZoomMax
Variants: 500 mg, 10 count blister
Lot Numbers:
YZM240406 (Exp: 04/05/2027)

Distributed by: ZoomMax, Sacramento, CA

Product: ZapMax Capsules (500 mg)by ZapMax
Variants: 500 mg, 10 count blister
Lot Numbers:
YZM240406 (Exp: 04/05/2027)

Distributed by: ZapMax, Sacramento, CA

Product Images

ZoomMax capsules, 10 count blister pack, front label

ZoomMax capsules, 10 count blister pack, front label

ZoomMax capsules back label

ZoomMax capsules back label

ZapMax capsules, 10 count blister pack, front label

ZapMax capsules, 10 count blister pack, front label

ZapMax capsules back label

ZapMax capsules back label

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95714
Status: Active
Manufacturer: Boulla LLC
Sold By: vitalityxtra.com; PeakMax.com; zoommax.com; zapmax.com
Manufactured In: United States
Units Affected: 4 products (Unknown; Unknown; Unknown; Unknown)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท FDA Press Release ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.