FDAFDA recall H-0017-2027 · Oct 14, 2026
A&P CREATIONS: biQ-FEL recall
Recall found
Product
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 COLOMBIANA; Distributed by: Biofel
Reason for recall
Product contains undeclared Sildenafil and Tadalafil.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28
- Quantity
- 3,116 bottles
- Distribution
- Distributed nationwide (US).
- Recalling firm
- A&P CREATIONS, Clermont, FL
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-09-14
Source: openFDA enforcement record H-0017-2027 · search recall number H-0017-2027 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 21, 2026, 12:30 AM EDT. The agency notice is the final word.