GenoGenix LLC: Drug Recall

Recall # · 07/30/2025

Class II: Risk

Recall Details

Recall Number
Classification
Class II
Product Type
Drug
Recalling Firm
GenoGenix LLC
Status
Ongoing
Date Initiated
07/30/2025
Location
Boca Raton, FL, United States
Voluntary/Mandated
Voluntary: Firm initiated

Reason for Recall

Lack of Assurance of Sterility

Product Description

Retatrutide for Injection, 60mg / 10mL vial, all presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692

Distribution Pattern

US Nationwide.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.