The Recall Registry
Recall data checked 6 hours ago

Home Prescription medicine Hua Da Trading, Inc. dba Wefun Inc. — WEFUN…

Food & drug recall · FDAAugust 25, 2023Highest risk

Hua Da Trading, Inc. dba Wefun Inc. — WEFUN Capsules 825 mg, 1x10 blister pack per carton

Do not stop taking this without speaking to your pharmacist or doctor.

What’s wrong

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.

The Recall Registry rates this highest riskFDA Class I: reasonable probability of serious harm or death.

What to do

Check the lot numbers below against what you have. Do not stop taking a prescription medicine because of a recall without speaking to your pharmacist or doctor first — for many medicines stopping is more harmful than continuing, and they can tell you whether yours is affected and what to do about it.

Who to contact: Recalling firm: Hua Da Trading, Inc. dba Wefun Inc.

The product

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

Details

Units affected
300 cartons
Recall date
August 25, 2023
Brand
Hua Da Trading, Inc. dba Wefun Inc.
Model, lot or SKU numbers
Lot # #18520168, Exp. date 09/30/2026 .
Where it was distributed

Distributed Nationwide in the USA

The official notice

This recall was issued by the U.S. Food and Drug Administration. The Recall Registry summarises it — always confirm the details at the source.

Their exact wording: Hua Da Trading, Inc. dba Wefun Inc. — WEFUN Capsules 825 mg, 1x10 blister pack per carton, Manufactured by WEFUN Brooklyn NY 11204 www.eshoponlineusa.com Bar Code X00358V0O5

Read it on FDA

Worried about the other things in your house? You can write down what you have and be told if one is recalled — or, if you sell second-hand, check your whole stock at once.

Filed under: Prescription medicine

Other prescription medicine recalls