Terminated Class II

ProSupps USA LLC

Recall F-3591-2017 · Plano, TX

Product

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

Reason for recall

Product contains the unapproved ingredient, picamilon.

Distribution

US and Canada

Quantity affected

65,195 units

Recall type

Voluntary: Firm initiated

Lot / code info

A107911115, A110400216, X016652L1

Timeline

30 Aug 2017 initiated → 29 Sep 2017 classified → 11 Oct 2017 reported → 6 Feb 2018 terminated

Sourced directly from the FDA’s openFDA enforcement database. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.