VitalityXtra recalls 500mg capsules with undeclared sildenafil and diclofenac. Products may cause serious health risks without FDA approval. Check your lot number for affected items.
Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
VitalityXtra is recalling 500mg capsules sold in 10-count blister packs. The capsules contain undeclared sildenafil and diclofenac, which are not approved by the FDA and could cause serious health risks.
The capsules contain sildenafil (an erectile dysfunction medication) and diclofenac (a painkiller) without proper FDA approval. These substances can cause serious health issues like heart problems, bleeding, or interactions with other medications.
People who own or use VitalityXtra 500mg capsules in 10-count blister packs. Those with underlying health conditions or who take medications that interact with sildenafil or diclofenac are at higher risk.
Check for the product name 'VitalityXtra Capsules, 500 mg', packaged in 10-count blister packs. The lot number is 230811 with an expiration date of 08/11/2025.
Immediately stop using the recalled VitalityXtra 500mg capsules as they contain undeclared sildenafil and diclofenac.
The capsules contain undeclared sildenafil and diclofenac without FDA approval, which could cause serious health risks.
Check for the product name 'VitalityXtra Capsules, 500 mg' in 10-count blister packs with lot number 230811 and expiration date 08/11/2025.
Immediately stop using the product and contact VitalityXtra for further instructions.
We’ve drafted a message you can send VitalityXtra to request your refund or repair — edit it as you like.
Subject: Recall D-0083-2025 — VitalityXtra VitalityXtra Hello, I own a VitalityXtra that is covered by recall D-0083-2025 from VitalityXtra. 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.
