Is DNPX Powder, 30 Green Apple recalled?

Product contains the unapproved ingredient, picamilon. Status: Voluntary: Firm initiated Initial Firm Notification: Letter Distribution: US and Canada

Medium RiskFDA Food

ProSupps USA LLC: Product contains the unapproved ingredient, picamilon.

Agency Publication Date: September 29, 2017

Affected Products

Product: DNPX Powder, 30 Green Apple

A106770915

Product: Mr. Hyde Green Apple domestic sample pack

A106971015

Product: Mr. Hyde Fruit Punch Canada; Mr. Hyde V2 Fruit Punch domestic

A107101015, A110280216, A110340216, A111110316, RLA106950915, XA105210815, X017290L4, X017291L4, 7291555, A106890915R, P1327855F

Product: Dr. Jekyll 30 Watermelon; Dr. Jekyll Watermelon V2 domestic

A107311015, A108371215, A111520316, RLA103290615

Product: Mr. Hyde 60 Blue Razz; Hyde V2 Blue Razz; Mr. Hyde V2 international Blue Razz sample pack; Mr. Hyde Domestic V2 Blue Razz sample packs

A107621015, A109220116, A109380116, A109780116, A110360216, A111150316, XA104800715, XA105490815, 7291554, 11151117, P1427855F

Product: Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs

A107911115, A110400216, X016652L1

Product: Dr. Jekyll V2 Mango Passion Fruit Domestic 30; Dr. Jekyll Mango Passion Fruit V2 domestic

A107921115, XA105840815

Product: Mr. Hyde Mango Passion Fruit sample packs; Hyde V2 Mango Passion Fruit

A108961215, A109091215, RL017905L3

Product: Hyde V2 Cherry Bomb

A109101215, XA105220815

Product: Hyde V2 Berry Blast

A109121215, XA102900615

Product: Hyde V2 Watermelon; Mr. Hyde V2 Watermelon International 30; Mr. Hyde V2 Watermelon Domestic 60

A109131215, A109430116, A110540216, RL017907L6A, XA105170815, XA105180815, 7291556, XA10772115, XA105640815, 109110L6

Product: Hyde V2 Orange Burst

A109151215

Product: Dr. Jekyll V2 international Blue Razz sample packs, Dr. Jekyll Blue Razz V2 domestic

A109660116, X016662L1, X0166624

Product: Dr. Jekyll Green Apple V2 domestic

RLA105850815

Product: DNPX Powder, 30 Pineapple Punch

RLA134860315, RL105080815, RL134660315

Product: DNPX Powder, 30 Blue Razz

RLA106760915

Product: Vanish V3

XCA105620815

Product: Dr. Jekyll Fruit Punch Domestic

RLA103280615

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 78043

Status: Resolved

Manufacturer: ProSupps USA LLC

Manufactured In: United States

Units Affected: 18 products (694 units; 25,318 units; 30,842 units; 34,387 units; 175,299 units; 65,195 units; 2508 units; 26,564 units; 4483 units; 3803 units; 22,505 units; 2147 units; 3,727 units; 1,827 units; 40 units; 2 units; 573 units; 6167 units)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.