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 tablets Recalled by Wockhardt Usa Inc. Due to Failed Impurities/Degradation Specifications: 5mg strength being recalled for...

Date: August 22, 2017
Company: Wockhardt Usa 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 Wockhardt Usa Inc. directly.

Affected Products

Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India, Distributed by: Wockhardt, USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054, USA. NDC: 64679-924-03;

Quantity: 5050 bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Wockhardt Usa Inc.

Wockhardt Usa Inc. has 45 total recalls tracked by RecallDetector.

Related Recalls

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