ULTRA-STEN Rapid Size and Strength capsules — Class I drug recall D-1084-2017
Terminated recall by HARDCORE FORMULATIONS, reported 2017-08-23, distributed nationwide. Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
| Recall number | D-1084-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | HARDCORE FORMULATIONS, San Marcos, TX, United States |
| Recall initiated | 2017-07-05 |
| Classified | 2017-08-14 |
| Reported by FDA | 2017-08-23 |
| Terminated | 2020-10-05 |
| Distributed | Nationwide (US) |
| Quantity | 1,490 bottles |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00748252687630 |
Product
ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
Reason for recall
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
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/D-1084-2017. 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.