X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro
Summary
The FDA issued a Class I for X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC by A&P CREATIONS. Reason: Product contains undeclared Sildenafil and Tadalafil..
Details
Source
Food Recall
External ID
H-0016-2027
Action Date
2026-10-14
Status
Ongoing
Category
food
Product Description
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.
Lot/Code Info: Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
Quantity Affected: 1,283 retail units
Reason for Recall
Product contains undeclared Sildenafil and Tadalafil.
Distribution
Distributed nationwide (US).
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-14
Company
Clermont, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 35 food recalls issued in the same week, part of 92 food-related FDA actions this month.
A&P CREATIONS has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (A&P CREATIONS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does A&P CREATIONS have FDA actions?
A&P CREATIONS has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0016-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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