Class IITerminated in FDA datasetRecall initiated Aug 30, 2017

Mr. Hyde 60 Blue Razz; Hyde V2 Blue Razz; Mr. Hyde V2 international Blue Razz sample pack; Mr.…

Recalling firm: ProSupps USA LLC

Why it was recalled

Product contains the unapproved ingredient, picamilon.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 6, 2018.

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

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Original FDA recall reason

Product contains the unapproved ingredient, picamilon.

Recall details

Recall number
F-3590-2017
Event ID
78043
FDA status
Terminated
Initiated
Aug 30, 2017
Reported
Oct 11, 2017
Classified
Sep 29, 2017
Terminated
Feb 6, 2018
Quantity
175,299 units
Location
Plano, TX, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

US and Canada

FDA source record · F-3590-2017

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

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