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FDA · Drugs ·

Furosemide Tablets recall

Leading Pharma, LLC recalled Furosemide Tablets on April 29, 2026 because of cGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit. It was sold nationwide.

Why it was recalled

CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.

What's recalled

Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01

Quantity: 9384 bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Leading Pharma, LLC, Fairfield, NJ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0486-2026
Source
U.S. Food and Drug Administration

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