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FDA · Drugs ·

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride recall

Wells Pharma of Houston LLC recalled fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride on May 6, 2026 because of cGMP deviations. It was sold nationwide.

Why it was recalled

cGMP deviations.

What's recalled

fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.

Quantity: 50 syringes

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
Wells Pharma of Houston LLC, Houston, TX
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
U.S. Nationwide.
Status
Ongoing
Recall number
D-0508-2026
Source
U.S. Food and Drug Administration

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