FDA recall, , High risk
Erotic Enhancers WAP Sensual Enhancement Capsules
WAP Sensual Enhancement Capsules contain undeclared sildenafil, tadalafil, and flibanserin, which can lower blood pressure to dangerous levels.
Summary by Recall Canary from the FDA notice
What happened
Erotic Enhancers is voluntarily recalling WAP Sensual Enhancement Capsules, marketed as a dietary supplement for sexual enhancement, because the product was found to contain undeclared sildenafil, tadalafil, and flibanserin. The agency stated that the product was marketed without an approved NDA/ANDA. The recall, which began on May 6, 2026, was announced by the company on May 11, 2026, and added to the FDA's Enforcement Report on October 8, 2026.
The capsules were distributed nationwide in the USA via the internet on ebay.com. The recall is to the consumer level.
What to do
If the UPC on your package is listed below:
- Consumers that have WAP Sensual Enhancement which is being recalled should stop using the product.
- Dispose of it.
- Consumers with questions regarding this recall can contact Best Supplements Best Prices at eroticenhancers@
gmail.com or by calling 818-856-2141 Monday - Saturday 9am-5pm. - Contact your physician or healthcare provider if you have experienced any problems that may be related to taking or using this drug product.
Is yours affected?
Affected if its UPC is listed.
The company's latest announcement of May 11, 2026 covers all lots, so no lot or date is listed here.
A UPC is the number printed under a barcode.
WAP Sensual Enhancement Capsules
- UPC
- 80174 00462
- UPC
- 6 80174 00463 1
Recall details
- Company began the recall
- Sold in
WAP Sensual Enhancement UPC: 80174 00462 was marketed as a dietary supplement for sexual enhancement and was distributed nationwide in the USA via the internet on www.ebay.com.
- Company
- Erotic Enhancers
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that taking it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 99029
- Recall number
- D-0071-2027
- Quantity recalled
- 6 blister packs
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Classified by FDA
Summary updated
