Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Dexamethasone Elixir Recalled by Morton Grove Pharmaceuticals, Inc. Due to Failed Impurities/Degradation Specifications: higher than permissible levels of...

Date: February 21, 2022
Company: Morton Grove Pharmaceuticals, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Morton Grove Pharmaceuticals, Inc. directly.

Affected Products

Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.

Why Was This Recalled?

Failed Impurities/Degradation Specifications: higher than permissible levels of unknown impurities were found in the drug product.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Morton Grove Pharmaceuticals, Inc.

Morton Grove Pharmaceuticals, Inc. has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report