biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil
A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as Class I because the product contains undeclared Sildenafil and Tadalafil, which presents a reasonable probability of serious adverse health consequences. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
A&P CREATIONS is recalling biQ-FEL, a 16.9 fl oz (500 mL) beverage, because the product contains undeclared Sildenafil and Tadalafil. The recall involves 3,116 bottles manufactured by ALMENAT SAS and distributed by Biofel.
The affected product was distributed nationwide in the United States. The recall covers two specific lots: Lot # biQ-f001-06-25 with an expiry date of 05/06/2027, and Lot # biQ-003-01-26 with an expiry date of 01/01/28.
Consumers should check their inventory for these specific lot numbers and stop using the product if it matches the recalled description.
The recalled product
- 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
- Manufacturer
- A&P CREATIONS
- Category
- Food — Beverage
- Hazard
- Affected units
- 3,116
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot # biQ-f001-06-25
- Expiry: 05/06/2027
- Lot # biQ-003-01-26
- Expiry: 01/01/28
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · A&P CREATIONS
See all →- SevereFDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil
FDA (Food) · 2026-10-14
Same hazard · undeclared drug
See all →- SevereFDA Recalls Flower Power Female Enhancement for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2024-05-01
- SevereSamurai-X Honey 6800 Recalled for Undeclared Drug Ingredients
FDA (Drugs) · 2024-05-01
- SevereDietary supplement found to contain undeclared pharmaceutical drug tadalafil
FDA (Drugs) · 2022-07-27
- ModerateNOW Bee Pollen 500mg Capsules Recalled for Metronidazole Contamination
FDA (Food) · 2021-11-17
- ModerateNOW Royal Jelly supplements may contain undeclared Metronidazole
FDA (Food) · 2021-11-17
Similar recalls
- CriticalFDA Recalls Natural Herbal Coffee AMPT for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2017-12-27
- SevereFDA Recalls X10 Supplement Containing Undeclared Sildenafil and Tadalafil
FDA (Food) · 2026-10-14
- CriticalFDA Recalls Black Label X Capsules for Undeclared Sildenafil
FDA (Drugs) · 2016-12-28
- CriticalCaverFlo Natural Herbal Coffee Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2017-08-30
- CriticalExtenZe 600 mg Recalled for Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2014-05-28
- CriticalFDA Recalls 7K Capsules Containing Undeclared Sildenafil and Tadalafil
FDA (Drugs) · 2018-06-06