FDA Food recall · Reported October 11, 2017
DNPX Powder, 30 Green Apple
Product contains the unapproved ingredient, picamilon.
ProSupps USA LLC recalled DNPX Powder, 30 Green Apple - a moderate-severity action.
DNPX Powder, 30 Green Apple was recalled by ProSupps USA LLC in October 11, 2017. Reason: Product contains the unapproved ingredient, picamilon.. Check the official notice for the remedy. Verify recall #F-3586-2017 with the FDA Food before acting.
The recall
ProSupps USA LLC issued this moderate-severity FDA Food recall-Product contains the unapproved ingredient, picamilon..
- Moderate
- severity level
- 694 units
- affected scope
- Class II
- classification
- October 11, 2017
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-3586-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category - 25,457 food recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
DNPX Powder, 30 Green Apple
Reason for recall
Product contains the unapproved ingredient, picamilon.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-3586-2017 |
| Date reported | October 11, 2017 |
| Date initiated | August 30, 2017 |
| Recalling firm | ProSupps USA LLC |
| Firm location | Plano, TX |
| Affected scope | 694 units |
| Distribution | US and Canada |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-3586-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Why was this product recalled? ▼
Which agency issued this recall? ▼
Where was the recalled product distributed? ▼
What are the health risks of consuming a recalled food product? ▼
Nationwide recalls with similar severity or category timing
Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Food · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Compare this recall with Grade A White In-shell Chicken eggs packaged in the followi… → · All Food recalls
Methodology · Corrections · Archive as of August 2026