biQ-FEL recall — A&P CREATIONS
Product contains undeclared Sildenafil and Tadalafil.
Company / brand: A&P CREATIONS recalls
Affected product: biQ-FEL recall status
Official ID H-0017-2027 · Official record ↗
Notice names this product. A&P CREATIONS’s biQ-FEL is named in FDA Class I recall H-0017-2027. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Product contains undeclared Sildenafil and Tadalafil. Identifying details: Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28. Units affected: 3,116 bottles. Status: Ongoing.
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.
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
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.
Product contains undeclared Sildenafil and Tadalafil.
Company / brand: A&P CREATIONS recalls
Affected product: biQ-FEL recall status
Official ID H-0017-2027 · Official record ↗
See all A&P CREATIONS recalls →
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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.