Class IITerminated · reported 2017-10-11

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

ProSupps USA LLC recalled this product and the FDA reported the enforcement action on 11 October 2017 as Class II. The recall was initiated by the firm. Product contains the unapproved ingredient, picamilon.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

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
Reason for recall
Product contains the unapproved ingredient, picamilon.
Recalling firm
ProSupps USA LLC
Firm location
Plano, Texas, United States
Classification
Class II
Status
Terminated
Recall number
F-3590-2017
Quantity
175,299 units
Distribution
US and Canada
Initiated
30 August 2017
Reported by FDA
11 October 2017
Terminated
6 February 2018
Firm notified by
Letter
Product codes
A107621015, A109220116, A109380116, A109780116, A110360216, A111150316, XA104800715, XA105490815, 7291554, 11151117, P1427855F

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 18 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 18 separate recalls, which almost every published figure does, overstates it by a factor of 18. All 18 of them are listed on this page.
  • The recall ran for 5 months, from 30 August 2017 to termination on 6 February 2018. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
  • The FDA published the enforcement report 6 weeks after the firm began the recall.
  • The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

What this recall was for

Unapproved ingredients

An unapproved ingredient recall means a product contained a substance not permitted in food, most often an undisclosed pharmaceutical active found in a dietary supplement.

A preventive controls plan covers an unapproved ingredient under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 111
Dietary supplement CGMP: the identity, purity, strength and composition specifications a supplement manufacturer sets and verifies for every component and finished batch.
21 CFR 117 subpart G
Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.

Every product in this recall

The FDA opened 18 enforcement records for this one recall, one per product code. This page carries all of them; the 17 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 17 records of FDA event 78043
ReportedProductFirmReasonClass
2017-10-11Dr. Jekyll 30 Watermelon; Dr. Jekyll Watermelon V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Mr. Hyde Mango Passion Fruit sample packs; Hyde V2 Mango Passion FruitProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll Fruit Punch DomesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll V2 Mango Passion Fruit Domestic 30; Dr. Jekyll Mango Passion Fruit V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Cherry BombProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11DNPX Powder, 30 Green AppleProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll Green Apple V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Watermelon; Mr. Hyde V2 Watermelon International 30; Mr. Hyde V2 Watermelon Domestic 60ProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Mr. Hyde Fruit Punch Canada; Mr. Hyde V2 Fruit Punch domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Vanish V3ProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Berry BlastProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11DNPX Powder, 30 Pineapple PunchProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll V2 international Blue Razz sample packs, Dr. Jekyll Blue Razz V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Orange BurstProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Mr. Hyde Green Apple domestic sample packProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11DNPX Powder, 30 Blue RazzProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packsProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II

Other records from ProSupps USA LLC

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 31 other records name this firm.

ReportedProductFirmReasonClass
2017-10-11Dr. Jekyll 30 Watermelon; Dr. Jekyll Watermelon V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Mr. Hyde Mango Passion Fruit sample packs; Hyde V2 Mango Passion FruitProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll Fruit Punch DomesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll V2 Mango Passion Fruit Domestic 30; Dr. Jekyll Mango Passion Fruit V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Cherry BombProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11DNPX Powder, 30 Green AppleProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Dr. Jekyll Green Apple V2 domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Hyde V2 Watermelon; Mr. Hyde V2 Watermelon International 30; Mr. Hyde V2 Watermelon Domestic 60ProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Mr. Hyde Fruit Punch Canada; Mr. Hyde V2 Fruit Punch domesticProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II
2017-10-11Vanish V3ProSupps USA LLCProduct contains the unapproved ingredient, picamilon.Class II

All 32 records for ProSupps USA LLC

All 2017 recalls · All FDA food recall data

21 CFR 111 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.