Mr. Hyde, Fruit Punch, 30 servings; Mr. Hyde Fruit Punch (V2); Mr. Hyde 30 INT'L Fruit…
ProSupps USA LLC recalled this product and the FDA reported the enforcement action on 5 July 2017 as Class II. The recall was initiated by the firm. Product is potentially mislabeled and contains the non-dietary 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, Fruit Punch, 30 servings; Mr. Hyde Fruit Punch (V2); Mr. Hyde 30 INT'L Fruit Punch; Mr. Hyde Fruit Punch RTD; Mr. Hyde V2 domestic Fruit Punch
- Reason for recall
- Product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
- Recalling firm
- ProSupps USA LLC
- Firm location
- Plano, Texas, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-2401-2017
- Quantity
- 37,983 units
- Distribution
- US and Canada
- Initiated
- 16 May 2017
- Reported by FDA
- 5 July 2017
- Terminated
- 6 February 2018
- Firm notified by
- Letter
- Product codes
- A107131015, A107561015; A109420116, 153500346, 153510266, A109400116
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 8 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 8 separate recalls, which almost every published figure does, overstates it by a factor of 8. All 8 of them are listed on this page.
- The recall ran for 9 months, from 16 May 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 7 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
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen 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 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 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 8 enforcement records for this one recall, one per product code. This page carries all of them; the 7 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.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2017-07-05 | Mr. Hyde Blue Razz (V2) | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Mr. Hyde Watermelon (V2); Mr. Hyde 30 Watermelon | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Dr. Jekyll V2 Orange Burst domestic | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Dr. Jekyll V2 Watermelon domestic | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Dr. Jekyll 30 Fruit Punch | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Dr. Jekyll V2 Green Apple International | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary ingredient Picamilon. | Class II |
| 2017-07-05 | Mr. Hyde Green Apple; Mr. Hyde Green Apple Sweden | ProSupps USA LLC | Product is potentially mislabeled and contains the non-dietary 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.
All 32 records for ProSupps USA LLC
All 2017 recalls · All FDA food recall data
21 CFR 117.135(c)(2) 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 accessRecall 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.