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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77208

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
May 05, 2017
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Genetic Edge Compounds 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

1 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 1

GEC LX Laxoplex 60 capsules Dietary Supplement, 60 count bottle, Manufactured by GEC, McKinney, TX, 75070, UPC: 700580499842

D-1092-2017
Recall number
D-1092-2017
Initiated
May 05, 2017
Classification
Class I
Status
Terminated
Quantity
1759 bottles ( 105, 540 capsules)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic steroids and steroid like substances.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary Supplement: FDA analysis found the product to tainted with undeclared anabolic steroids and steroid like substances.

Code information

All lots.

Distribution pattern

Nationwide

Field note

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