ZoomMax recalls 500mg capsules with undeclared sildenafil and diclofenac. Consumers should stop using these products due to unapproved ingredients.
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
ZoomMax is recalling 500mg capsules that contain undeclared sildenafil and diclofenac, which are not approved for use in the U.S. This poses a risk of serious health issues due to the unapproved ingredients.
These capsules contain sildenafil (an erectile dysfunction medication) and diclofenac (a painkiller) without proper FDA approval. Using them can cause serious health problems like heart issues or allergic reactions.
Anyone who owns or uses ZoomMax 500mg capsules. People with underlying health conditions or those taking other medications are at higher risk.
Check for ZoomMax 500mg capsules in 10-count blister packs. The lot number YZM240406 was distributed by ZoomMax in Sacramento, CA.
Immediately stop using the recalled ZoomMax 500mg capsules as they contain unapproved ingredients that can cause serious health risks.
The capsules contain undeclared sildenafil and diclofenac without FDA approval, which can cause serious health issues.
Check for ZoomMax 500mg capsules in 10-count blister packs with lot number YZM240406.
Stop using the product immediately and contact ZoomMax for further instructions.
We’ve drafted a message you can send ZoomMax to request your refund or repair — edit it as you like.
Subject: Recall D-0085-2025 — ZoomMax ZoomMax Hello, I own a ZoomMax that is covered by recall D-0085-2025 from ZoomMax. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
