Independent recall search Not a government website Verify instructions at the issuing-agency source
FDA source record Class I Ongoing

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

Recall Date: 2026-09-14 Recalling Firm: A&P CREATIONS Record Ref: H-0017-2027

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 and names A&P CREATIONS as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: A&P CREATIONS
  • Classification: Class I
  • Status: Ongoing
  • Recall date: 2026-09-14
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

FDA public announcements can appear before an enforcement report is classified, so an empty classification does not mean the notice is unimportant.

Product Description & Identification

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 / Hazard Identified

Product contains undeclared Sildenafil and Tadalafil.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

Verify product details with official government notices before taking action.

Distribution & Affected States

Distributed nationwide (US).

Verify With the Issuing Agency

This record was last updated in our index on 2026-10-29 00:15:03 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

Open FDA Source Record →

Record Transparency

Issuing agency
FDA
Source ID
H-0017-2027
Indexed update
2026-10-29 00:15:03 UTC
Official source
Open issuing-agency record