FDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling X10 Natural Enhancement Supplement because it contains undeclared Sildenafil and Tadalafil.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this recall as Class I because the product contains undeclared Sildenafil and Tadalafil, which can cause serious adverse health consequences. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
A&P CREATIONS is recalling X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box. The recall involves 1,283 retail units distributed nationwide in the United States.
The product is being recalled because it contains undeclared Sildenafil and Tadalafil. These are active pharmaceutical ingredients that are not listed on the product label.
Consumers should stop using the product and return it to the place of purchase for a refund. The affected lots are F090824LN16, F170325LN19, and 300326LN28.
The recalled product
- Product
- X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.
- Manufacturer
- A&P CREATIONS
- Category
- Food — Dietary Supplement
- Affected units
- 1,283
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (6)
- Lot # F090824LN16
- Expiry: 8/2026
- Lot # F170325LN19
- Expiry: 03/2027
- Lot # 300326LN28
- Expiry: 03/2028.
Distribution
Distributed nationwide across the United States.
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