FDA recall D-1699-2012

Product

Man King Capsules, 2800 mg, boxes of 5 packets, OTC, Developed by: American Wanbao Pharmaceutical International Group and Hainan Wanbao Biological Engineering Co., Ltd., 27 Heping Road, Haikou, Henan Province, UPC 9 009900 0032328

Reason for recall

Marketed Without an Approved ANDA/NDA: presence of sildenafil.

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2012-02-23

Report date

2012-10-03

Termination date

2018-11-01

Voluntary/Mandated

Voluntary: Firm initiated

Location

Brewerton, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1699-2012