# FDA recall D-1180-2023

> **Hua Da Trading, Inc. dba Wefun Inc.** · Class I · drug recall initiated 2023-08-25.

## Product

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

## 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.

## Distribution

Distributed Nationwide in the USA

## Key facts

- **Recall number:** D-1180-2023
- **Recalling firm:** Hua Da Trading, Inc. dba Wefun Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-08-25
- **Report date:** 2023-09-20
- **Termination date:** 2026-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1180-2023

## Citation

> AI Analytics. FDA recall D-1180-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-1180-2023. Source: US FDA. Licensed CC0.

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