D-0800-2020 Class II Terminated

Recalled by Tuscano and Delucia Group (DBA Entropic Labs) — Salt Lake City, UT

FDA drug recall D-0800-2020 was initiated by Tuscano and Delucia Group (DBA Entropic Labs) on August 24, 2019 and is designated Class II. Reason for recall: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen Receptor Modulators (SARMs) The recall status is terminated (terminated July 12, 2023). Affected quantity: 60.

Recall Details

Product Type
Drugs
Report Date
January 29, 2020
Initiation Date
August 24, 2019
Termination Date
July 12, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
60

Product Description

Entropic Labs SARM RAD-140, 20mg Capsules, 30-count bottles, Entropic Labs UPC#: 651074545302

Reason for Recall

Marketed Without An Approved NDA/ANDA: product contains Selective Androgen Receptor Modulators (SARMs)

Distribution Pattern

Nationwide within the United States

Code Information

All lots