Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77664

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

Open FDA event record

Event summary

Timeline bucket
June 06, 2017
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Andropharm, LLC

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

ANDROPHARM STEN Z (2, 17a-Dimethyl-17b-hydroxy-5a-androst-1-en-3-one 10mg and 17b-hydroxy-2a, 17b-dimethyl-5a-androstan-3-one azine 10 mg) capsule, packaged in 60-count bottle, Andropharm.com, UPC: 6 42125 50294 8

D-1142-2017
Recall number
D-1142-2017
Initiated
June 06, 2017
Classification
Class I
Status
Terminated
Recalling firm
Andropharm, LLC
Quantity
150 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

Code information

All lots remaining within expiry.

Distribution pattern

Florida

drug · product 2 of 2

ANDROPHARM M1 ALPHA (Methyl-1-Etiocholenolol-Epietiocholanollone 20 mg) capsule, packaged in 60-count bottle, Amazon.com, UPC 6 42125 50292 4

D-1143-2017
Recall number
D-1143-2017
Initiated
June 06, 2017
Classification
Class I
Status
Terminated
Recalling firm
Andropharm, LLC
Quantity
1250 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without an approved NDA/ANDA: product label states it contains anabolic steroids.

Code information

All lots remaining within expiry.

Distribution pattern

Florida