CLASS I ONGOING Food recall · Reported 14 Oct 2026 · FDA Enforcement Report
X10 Natural Enhancement Supplement, 7 sachets/box recalled
A&P Creations is recalling X10 Natural Enhancement Supplement, 7 sachets/box, 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-0016-2027
- 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
- Dietary Supplements
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
X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by FutuPro S.A.S., Colombian Industry; Distributed by Natur Fuel, 2725 Armstrong Avenue, Clermont, FL 34714.
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 # F090824LN16, Expiry: 8/2026; Lot # F170325LN19, Expiry: 03/2027; Lot # 300326LN28, Expiry: 03/2028.
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 99872| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | biQ-FEL recalled by A&P Creations | A&P Creations | Undeclared Allergens | Nationwide |
More recalls from A&P Creations
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | biQ-FEL recalled by A&P Creations | A&P Creations | Undeclared Allergens | Nationwide |
| Food | ANNOUNCED | biQ-FEL supplement recalled by A&P CreationsbiQ-FEL | A&P Creations | Hidden Drug Ingredients |
Other Dietary Supplements recalls
All 735| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Amino Ultra, dietary supplement in white recalledAmino Ultra | Evexias Health Solution | Undeclared Fish & Shellfish | 9 states |
| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
| Food | CLASS I | Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR | ZMB Enterprises | Hidden Drug Ingredients | CA |
| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |