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Class I FDA

A&P CREATIONS recalls 2 products over undeclared drug ingredient

Status: Ongoing · Recalled September 14, 2026 · Updated October 20, 2026
A&P CREATIONS recalled 2 products on September 14, 2026 because of undeclared drug ingredient. It is a Class I recall (reasonable probability of serious harm or death). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Products2
HazardUndeclared drug ingredient
Risk levelClass I
Affected areaNationwide

What to do

Do not eat this product. Check the official FDA notice for affected lot codes and instructions.

Confirm the details against the official FDA notice before acting.

Recalled products (2)

Check the product in your home against each recalled item:

  1. X10 Natural Enhancement Supplement

    Product as filed
    A&P CREATIONS — X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian…
    Lot & date codes
    Lot # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
    Quantity
    1,283 retail units
  2. biQ-FEL

    Product as filed
    A&P CREATIONS — biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA…
    Lot & date codes
    Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28
    Quantity
    3,116 bottles

Full recall details

Reason for recall
  • Clermont, Florida – A&P Creations LLC is recalling X10 Natural Enhancement Supplement to the consumer level because it has been found to contain undeclared sildenafil and tadalafil.
  • Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional.
Hazard class
Class I — reasonable probability of serious harm or death
Recalling company
A&P CREATIONS
Recall type
Voluntary: Firm initiated
Distribution
Distributed nationwide (US).

Compiled from the official FDA records by our data rules — how we build these pages. Spotted an error? Report it.

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