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fentaNYL Citrate Injectable Solution recall

FDA recall D-0503-2026 · initiated Apr 1, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated May 6, 2026How we research

Wells Pharma of Houston LLC recalled fentaNYL Citrate Injectable Solution in Apr 2026 — an FDA Class II recall (D-0503-2026) because cGMP deviations.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

cGMP deviations.

The manufacturing process itself

The FDA found the process itself out of compliance, usually before any defective product was identified.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

120925202022769, Expiration Date 04/09/2026, 123125202022883, Expiration Date 05/05/2026, 123125202022884, Expiration Date 05/05/2026 011226202020057, Expiration Date 05/14/2026, 011226202020058, Expiration Date 05/14/2026, 011626202020110, Expiration Date 05/20/2026 012726202020156, Expiration Date 05/28/2026. 012726202020161, Expiration Date 05/28/2026 020226202020195, Expiration Date 06/04/2026 021826202020386, Expiration Date 06/20/2026 022026202020417, Expiration Date 06/24/2026 022026202020424 Expiration Date 06/24/2026

Quantity recalled: 4,030 IV Bags

Details

Product
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
Recalling company
Wells Pharma of Houston LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
U.S. Nationwide.
Initiated
Apr 1, 2026
FDA report date
May 6, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was fentaNYL Citrate Injectable Solution recalled?
Wells Pharma of Houston LLC recalled fentaNYL Citrate Injectable Solution in Apr 2026 — an FDA Class II recall (D-0503-2026) because cGMP deviations. May cause temporary or medically reversible harm; low probability of serious harm.
Why was fentaNYL Citrate Injectable Solution recalled?
Per the FDA enforcement record, the reason for recall D-0503-2026 was: cGMP deviations.
Is a recalled fentaNYL Citrate Injectable Solution dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of fentaNYL Citrate Injectable Solution are affected?
Distributed: U.S. Nationwide.. The recall covers these lots — 120925202022769, Expiration Date 04/09/2026, 123125202022883, Expiration Date 05/05/2026, 123125202022884, Expiration Date 05/05/2026 011226202020057, Expiration Date 05/14/2026, 011226202020058, Expiration Date 05/14/2026, 011626202020110, Expiration Date 05/20/2026 012726202020156, Expiration Date 05/28/2026. 0127262…. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0503-2026.

Source: openFDA Drug Enforcement record D-0503-2026

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