FDA Drug recall D-1180-2023
WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
- FDA Drug
- Class I
- terminated
- Published 2023-09-20
On 2023-09-20 the FDA classified a Class I recall of WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5 by Hua Da Trading, citing 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….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1180-2023 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2023-08-25 |
| Published | 2023-09-20 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Hua Da Trading |
| Distribution | US |
Product
WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
Reason
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.
Identifiers
| code_info | Lot # #18520168, Exp. date 09/30/2026 . |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1180-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.