Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Enalapril Maleate Recalled by Aidarex Pharmaceuticals LLC Due to Out-of-specification results for the Enalapril Diketopiperazine degradation product...

Date: June 27, 2018
Company: Aidarex Pharmaceuticals LLC
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 Aidarex Pharmaceuticals LLC directly.

Affected Products

Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30

Quantity: 25, 30-count bottles

Why Was This Recalled?

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Aidarex Pharmaceuticals LLC

Aidarex Pharmaceuticals LLC has 10 total recalls tracked by RecallDetector.

Related Recalls

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