WEFUN Capsules 825 mg recall
WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
Why was WEFUN Capsules 825 mg recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # #18520168, Exp. date 09/30/2026 .
- Product
- WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5
- Recalling firm
- Hua Da Trading, Inc. dba Wefun Inc.
- Quantity
- 300 cartons
- Distribution
- Distributed Nationwide in the USA
- Recall date
- September 20, 2023
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)