CLASS I ONGOING Food recall · Reported 14 Oct 2026 · FDA Enforcement Report
biQ-FEL recalled by A&P Creations
A&P Creations is recalling biQ-FEL per, distributed nationwide in the US. The recall was initiated on 14 Sep 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0017-2027
- FDA event ID
- 99872
- Recalling firm
- A&P Creations, Clermont, FL
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 14 Sep 2026
- FDA classified
- 7 Oct 2026
- Reported
- 14 Oct 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 14 Sep 2026 | Recall initiated by company | |
| 7 Oct 2026 | Classified by FDA | +23 days |
| 14 Oct 2026 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains undeclared Sildenafil and Tadalafil.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
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
Where it was distributed
Distributed nationwide (US).
Questions about this recall
Why was it recalled?
Product contains undeclared Sildenafil and Tadalafil.
Which lots are affected?
Lot # biQ-f001-06-25, Expiry: 05/06/2027; Lot # biQ-003-01-26, Expiry: 01/01/28
Where was it sold?
Distributed nationwide (US).
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 99872This product is part of a recall event; the main page for the event is X10 Natural Enhancement Supplement, 7 sachets/box recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | X10 Natural Enhancement Supplement, 7 sachets/box recalled | A&P Creations | Undeclared Allergens | Nationwide |
More recalls from A&P Creations
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | X10 Natural Enhancement Supplement, 7 sachets/box recalled | A&P Creations | Undeclared Allergens | Nationwide |
| Food | ANNOUNCED | biQ-FEL supplement recalled by A&P CreationsbiQ-FEL | A&P Creations | Hidden Drug Ingredients |
Other Other recalls
All 4,675| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC recalledElevated Edibles | Sweet Sensi | Other Bacterial Contamination | Nationwide |
| Food | ANNOUNCED | Para Bien Al Grano recalled by Pan PepinPara Bien | Pan Pepin | Undeclared Sesame | PR |
| Food | CLASS II | Mezzetta Golden Greek Peperoncini Medium Heat G.L. Mezzetta recalledMezzetta | G L Mezzetta | Foreign Material | 22 states |
| Food | ANNOUNCED | Pan Pepín Inc. Emite Alerta por Alérgenos en el Producto recalled | Other | ||
| Food | CLASS I | Alfalfa & Mung Bundle each), packaged separately recalledAlfalfa | Todd's Seeds | Salmonella | Nationwide |