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.

Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to Subpotent Drug.

Date: February 15, 2019
Company: Heritage 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 Heritage Pharmaceuticals, Inc. directly.

Affected Products

Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31

Quantity: 11888 units

Why Was This Recalled?

Subpotent Drug.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Heritage Pharmaceuticals, Inc.

Heritage Pharmaceuticals, Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

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