Fresh Recalls

FDAClass I · Food · Recall H-0016-2027 · Recalled October 14, 2026

X10 Natural Enhancement Supplement recall — A&P CREATIONS

Agency report date: October 14, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
X10 Natural Enhancement Supplement
Company / brand
A&P CREATIONS
Lot / serial / date codes
Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
Distribution
Distributed nationwide (US).
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Product contains undeclared Sildenafil and Tadalafil.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: X10 Natural Enhancement Supplement recall status

3. Open the official notice or contact

Official recall ID
H-0016-2027
Brand
All A&P CREATIONS recalls
Classification
Class I
Units affected
1,283 retail units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Clermont, FL, United States
Firm address
2725 Armstrong Ave, N/A, 34714-8117

Identifying details (verbatim from the notice)

Product codes / lots
Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
Distribution
Distributed nationwide (US).
Firm notified the public via
Press Release
FDA event ID
99872
Recall initiated
September 14, 2026
FDA classified
October 7, 2026
FDA report date
October 14, 2026

More A&P CREATIONS recalls

Other food recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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