FDA Drug recall D-1084-2017
ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
- FDA Drug
- Class I
- terminated
- Published 2017-08-23
On 2017-08-23 the FDA classified a Class I recall of ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0 by Hardcore Formulations, citing marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1084-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2017-07-05 |
| Published | 2017-08-23 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hardcore Formulations |
| Distribution | US |
Product
ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0
Reason
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.
Identifiers
| upc | 748252687630 |
|---|---|
| code_info | All lots remaining within expiry. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1084-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.