Class IITerminated in FDA datasetAug 30, 2017

Dr. Jekyll Fruit Punch Domestic

Recalling firm: ProSupps USA LLC

Why it was recalled

Product contains the unapproved ingredient, picamilon.

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The exact product

Dr. Jekyll Fruit Punch Domestic

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Original FDA code information

RLA103280615

Recall details

Recall number
F-3603-2017
Event ID
78043
FDA status
Terminated
Initiated
Aug 30, 2017
Reported
Oct 11, 2017
Classified
Sep 29, 2017
Terminated
Feb 6, 2018
Quantity
6167 units
Location
Plano, TX, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US and Canada

FDA source record · F-3603-2017

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.