D-0567-2018 Class I Terminated

Recalled by A&H Focal Inc. — Staten Island, NY

Recall Details

Product Type
Drugs
Report Date
February 7, 2018
Initiation Date
March 7, 2017
Termination Date
June 14, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
unknown

Product Description

YANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language

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.

Distribution Pattern

NY and NJ through six retail stores named "Asian Food Markets"

Code Information

All Lots