Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77660

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 05, 2017
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
HARDCORE FORMULATIONS

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 2

ULTRA-STEN Rapid Size and Strength capsules, 10 mgs, 90 count bottle, Hardcore Formulations UPC: 7 48252 68763 0

D-1084-2017
Recall number
D-1084-2017
Initiated
July 05, 2017
Classification
Class I
Status
Terminated
Recalling firm
HARDCORE FORMULATIONS
Quantity
1490 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide

drug · product 2 of 2

D-ZINE Rapid Size and Strength capsules, 10mgs, 90 count bottle, Hardcore Formulations, UPC: 7 48252 86193 1

D-1085-2017
Recall number
D-1085-2017
Initiated
July 05, 2017
Classification
Class I
Status
Terminated
Recalling firm
HARDCORE FORMULATIONS
Quantity
1440 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Approved NDA/ANDA: Product contains Methylstenbolone or Dymethazine.

Code information

All lots remaining within expiry.

Distribution pattern

Nationwide