Recall Register

Food recall: DNPX Powder, 30 Green Apple

Class II FDA enforcement event 78043. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Product contains the unapproved ingredient, picamilon.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

ProSupps USA LLC started this food recall on 30 Aug 2017. The firm address in the FDA record is in Plano, TX. FDA put the recall in Class II. FDA event 78043 has 18 product records. The first FDA enforcement report date is 11 Oct 2017. The record gives the status Terminated, with the termination date 6 Feb 2018.

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.

US and Canada

Recalling firm

ProSupps USA LLC, Plano, TX.

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

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

Products

18 product records in the event.

FDA event 78043: product records
Recall numberProductQuantityClassStatusReport date
F-3586-2017DNPX Powder, 30 Green Apple694 unitsClass IITerminated11 Oct 2017
F-3587-2017Mr. Hyde Green Apple domestic sample pack25,318 unitsClass IITerminated11 Oct 2017
F-3588-2017Mr. Hyde Fruit Punch Canada; Mr. Hyde V2 Fruit Punch domestic30,842 unitsClass IITerminated11 Oct 2017
F-3589-2017Dr. Jekyll 30 Watermelon; Dr. Jekyll Watermelon V2 domestic34,387 unitsClass IITerminated11 Oct 2017
F-3590-2017Mr. Hyde 60 Blue Razz; Hyde V2 Blue Razz; Mr. Hyde V2 international Blue Razz sample pack; Mr. Hyde Domestic V2 Blue Razz sample packs175,299 unitsClass IITerminated11 Oct 2017
F-3591-2017Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs65,195 unitsClass IITerminated11 Oct 2017
F-3592-2017Dr. Jekyll V2 Mango Passion Fruit Domestic 30; Dr. Jekyll Mango Passion Fruit V2 domestic2508 unitsClass IITerminated11 Oct 2017
F-3593-2017Mr. Hyde Mango Passion Fruit sample packs; Hyde V2 Mango Passion Fruit26,564 unitsClass IITerminated11 Oct 2017
F-3594-2017Hyde V2 Cherry Bomb4483 unitsClass IITerminated11 Oct 2017
F-3595-2017Hyde V2 Berry Blast3803 unitsClass IITerminated11 Oct 2017
F-3596-2017Hyde V2 Watermelon; Mr. Hyde V2 Watermelon International 30; Mr. Hyde V2 Watermelon Domestic 6022,505 unitsClass IITerminated11 Oct 2017
F-3597-2017Hyde V2 Orange Burst2147 unitsClass IITerminated11 Oct 2017
F-3598-2017Dr. Jekyll V2 international Blue Razz sample packs, Dr. Jekyll Blue Razz V2 domestic3,727 unitsClass IITerminated11 Oct 2017
F-3599-2017Dr. Jekyll Green Apple V2 domestic1,827 unitsClass IITerminated11 Oct 2017
F-3600-2017DNPX Powder, 30 Pineapple Punch40 unitsClass IITerminated11 Oct 2017
F-3601-2017DNPX Powder, 30 Blue Razz2 unitsClass IITerminated11 Oct 2017
F-3602-2017Vanish V3573 unitsClass IITerminated11 Oct 2017
F-3603-2017Dr. Jekyll Fruit Punch Domestic6167 unitsClass IITerminated11 Oct 2017

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 II: The middle of the three FDA recall classes.

The event in context

Food events that started in 2017
599
Share of these events in Class II
52%
Product records in this event
18Median of the firm: 8
Events of the firm on the register
4

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 78043. https://recallregister.com/fda/ii/78043/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 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: US and Canada
What quantity of product is in FDA event 78043?
The event has 18 product records. The first record gives this quantity: 694 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2017 have the same class?
52% of the 599 food events that started in 2017 are in Class II.