← FDA ENFORCEMENT
D-1180-2023Class I

Hua Da Trading, Inc. dba Wefun Inc.

Recalling firm
Hua Da Trading, Inc. dba Wefun Inc.
Product type
Drug
Status
Terminated
Report date
2023-09-20
Distribution
Distributed Nationwide in the USA
Firm state
NY
Product quantity
300 cartons
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil, an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

Product description

WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5

Code / lot info

Lot # #18520168, Exp. date 09/30/2026 .

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.