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.

Edex (alprostadil for injection) 10mcg Recalled by Endo Pharmaceuticals, Inc. Due to Lack of Assurance of Sterility: Defective container resulting...

Date: February 22, 2017
Company: Endo 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 Endo Pharmaceuticals, Inc. directly.

Affected Products

Edex (alprostadil for injection) 10mcg, packaged in a 2 pack carton, Rx only, Manufactured in Germany for: Actient Pharmaceuticals, LLC, Lake Forest, Illinois 60045; NDC 52244-010-02.

Quantity: 5,086 cartridges

Why Was This Recalled?

Lack of Assurance of Sterility: Defective container resulting in the lack of sterility assurance. ok thanks

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Endo Pharmaceuticals, Inc.

Endo Pharmaceuticals, Inc. has 5 total recalls tracked by RecallDetector.

Related Recalls

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