CLASS II Food recall · Reported 5 Jul 2017 · FDA Enforcement Report

Mr. Hyde Blue Razz (V2) recalled by ProSupps USA

ProSupps USA is recalling Mr. Hyde Blue Razz (V2). The recall was initiated on 16 May 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesA107141015, A107291015, A108741215
Quantity recalled34,124 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2403-2017
FDA event ID
77285
Recalling firm
ProSupps USA, Plano, TX
Classification
Class II
Status
Terminated
Recall initiated
16 May 2017
FDA classified
28 Jun 2017
Reported
5 Jul 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors
Product category
Other

Timeline

16 May 2017Recall initiated by company
28 Jun 2017Classified by FDA+43 days
5 Jul 2017Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.

Product as listed by the FDA

Mr. Hyde Blue Razz (V2)

Where it was distributed

US and Canada

Questions about this recall

Is Mr. Hyde Blue Razz (V2) recalled?

Yes. ProSupps USA recalled Mr. Hyde Blue Razz (V2) on 16 May 2017. The recall is Class II and its status is Terminated. Recall number F-2403-2017.

Why was it recalled?

Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.

Which lots are affected?

A107141015, A107291015, A108741215

Where was it sold?

US and Canada

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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