ZapMax recalls 500mg capsules due to undeclared sildenafil and diclofenac. Consumers should stop using these products immediately as they may contain harmful ingredients without FDA approval.
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
ZapMax is recalling 500mg capsules because they contain undeclared sildenafil and diclofenac without FDA approval. This poses a risk of serious health effects if taken without proper medical supervision.
These capsules contain sildenafil (an erectile dysfunction drug) and diclofenac (a painkiller) without proper FDA approval. Taking them without medical supervision could cause serious health issues like heart problems or allergic reactions.
Anyone who owns or uses ZapMax 500mg capsules. People with underlying health conditions or those taking other medications are at higher risk due to potential drug interactions.
Check for the product name 'ZapMax Capsules', 500 mg, 10 count blisters in cartons. The lot number YZM240406 and expiration date 04/05/2027 may also be visible on the packaging.
Immediately stop using the recalled capsules as they contain undeclared sildenafil and diclofenac without FDA approval.
The capsules contain undeclared sildenafil and diclofenac without FDA approval, which could cause serious health effects if taken without medical supervision.
Look for the product name 'ZapMax Capsules', 500 mg, 10 count blisters in cartons with lot number YZM240406 and expiration date 04/05/2027.
Stop using the capsules immediately and contact ZapMax at www.zapmax.com for further instructions.
We’ve drafted a message you can send ZapMax to request your refund or repair — edit it as you like.
Subject: Recall D-0086-2025 — ZapMax ZapMax Hello, I own a ZapMax that is covered by recall D-0086-2025 from ZapMax. 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.
