Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL

SOMERSET THERAPEUTICS LLC has recalled Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on February 4, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, with approximately 62190 vials affected. The company behind the recall is SOMERSET THERAPEUTICS LLC, based in Somerset, NJ. The FDA describes the product as: “Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, (10 mg/mL), 10x10 mL Multiple Dose Vials, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873, NDC carton: 70069-025-10; NDC vial: 70069-025-01”

Why was Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL recalled?

According to the FDA, the stated reason for the recall is: “Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.” In plain terms, this recall relates to a chemical impurity.

This recall involves an unwanted chemical detected in the medicine — often a nitrosamine impurity, which regulators limit because long-term exposure above set levels may increase health risks. Regulators recall affected batches as a precaution. Health authorities generally advise talking to a doctor or pharmacist before stopping a prescribed medicine.

What should you do?

If you think you may have bought Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, compare it against the product description and identifying codes (Lot #: A240421, Exp 07/31/2026) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact SOMERSET THERAPEUTICS LLC or your local health authority.

About this recall

This recall was distributed in NJ. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.