STREE OVERLORD capsules, 3800 mg, 4-count bottle, labeling is in foreign language
Recall Number: D-0564-2018
Firm: A&H Focal Inc.
Classification: Class II
Status: Terminated
Report Date: 20180207
Initiation Date: 20170307
Termination Date: 20190614
Reason for Recall
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.
Product Description
STREE OVERLORD capsules, 3800 mg, 4-count bottle, labeling is in foreign language