Recall Register

Food recall: X10 Natural Enhancement Supplement, 0.5 fl oz/sachet (15 mL), 7 sachets/box, UPC: 7708075247094, Manufactured by…

Class I FDA enforcement event 99872. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Product contains undeclared Sildenafil and Tadalafil.

Class I, in the words of FDA

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

A&P CREATIONS started this food recall on 14 Sep 2026. The firm address in the FDA record is in Clermont, FL. FDA put the recall in Class I. FDA event 99872 has 2 product records. The first FDA enforcement report date is 14 Oct 2026. The record gives the status Ongoing. 67 of the 339 food events that started in 2026 have more product records. The median food event of 2026 has 1 product record.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Distributed nationwide (US).

Recalling firm

A&P CREATIONS, Clermont, FL.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

2 product records in the event.

FDA event 99872: product records
Recall numberProductQuantityClassStatusReport date
H-0016-2027X10 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 34714.1,283 retail unitsClass IOngoing14 Oct 2026
H-0017-2027biQ-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: Biofel3,116 bottlesClass IOngoing14 Oct 2026

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Food events that started in 2026
339
Share of these events in Class I
40%
Product records in this event
2
Events of the firm on the register
1

Official channels

Cite this page

Recall Register. FDA enforcement event 99872. https://recallregister.com/fda/i/99872/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
27 Oct 2026
Newest FDA report date on the register
21 Oct 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Distributed nationwide (US).
What quantity of product is in FDA event 99872?
The event has 2 product records. The first record gives this quantity: 1,283 retail units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2026 have the same class?
40% of the 339 food events that started in 2026 are in Class I.