Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 30 SERVINGS WATERMELON NATURAL AND…
ProSupps USA LLC recalled this product and the FDA reported the enforcement action on 6 April 2016 as Class II. The recall was initiated by the firm. Product could be potentially mislabeled and contain 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
- Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 30 SERVINGS WATERMELON NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 7.5 OZ (213 GRAMS) and Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT WATERMELON NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 15.0 OZ (426 GRAMS) both packaged in red plastic jars with black lids.
- Reason for recall
- Product could be potentially mislabeled and contain non-dietary ingredient Picamilon.
- Recalling firm
- ProSupps USA LLC
- Firm location
- Plano, Texas, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1000-2016
- Quantity
- 3890 units
- Distribution
- Nationwide throughout the US including: PA, FL, NV, WI, UT, NC, CA, TX, OH, CT, VA, AZ, SC, IN, AR, GA, MS, CO, NJ
- Initiated
- 2 March 2016
- Reported by FDA
- 6 April 2016
- Terminated
- 1 February 2018
- Firm notified by
- Letter
- Product codes
- 110625 and 138201115
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 5 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 5 separate recalls, which almost every published figure does, overstates it by a factor of 5. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 5 of them.
- The recall ran for 23 months, from 2 March 2016 to termination on 1 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 distribution pattern names 18 states, and the FDA published the enforcement report 5 weeks after the firm began the recall.
- Recalls of a dietary supplement run a median of 15 months, so this one was longer than usual for its category. Dietary supplements are regulated under their own good manufacturing practice rule, 21 CFR part 111, and they are the only food category where the dominant recall reason is an ingredient that was never declared because it is a pharmaceutical.
Named in the distribution pattern: Florida, Nevada, Wisconsin, Utah, North Carolina, California, Texas, Ohio, Connecticut, Virginia, Arizona, South Carolina, Indiana, Arkansas, Georgia, Mississippi, Colorado, New Jersey. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
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.
Filed under dietary supplements. A product can sit in more than one.
Other dietary supplements recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
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 2016 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.