DNPX Powder — Class II food recall F-3601-2017
Terminated recall by ProSupps USA LLC, reported 2017-10-11. Product contains the unapproved ingredient, picamilon.
| Recall number | F-3601-2017 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ProSupps USA LLC, Plano, TX, United States |
| Recall initiated | 2017-08-30 |
| Classified | 2017-09-29 |
| Reported by FDA | 2017-10-11 |
| Terminated | 2018-02-06 |
| Countries outside the US | CA |
| Quantity | 2 units |
| Reason classes | unapproved product |
Product
DNPX Powder, 30 Blue Razz
Reason for recall
Product contains the unapproved ingredient, picamilon.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-3601-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.