RecallHawk
Class II Recall

fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC

Wells Pharma of Houston LLC

Summary

The FDA issued a Class II for fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per m by Wells Pharma of Houston LLC. Reason: cGMP deviations..

Details

Source

Drug Recall

External ID

D-0505-2026

Action Date

2026-05-06

Status

Ongoing

Category

drug

Product Description

fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC 73702-204-25.

Lot/Code Info: Lot 011226204250063, Exp Date 05/14/2026

Quantity Affected: 50 syringes

Reason for Recall

cGMP deviations.

Distribution

U.S. Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-01

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 65 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Wells Pharma of Houston LLC has 8 FDA actions in our database, including 8 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wells Pharma of Houston LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Wells Pharma of Houston LLC have FDA actions?

Wells Pharma of Houston LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0505-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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