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.

Captopril Tablets Recalled by Wockhardt Usa Inc. Due to CGMP Deviations: Firm did not adequately investigate customer...

Date: April 22, 2015
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

Captopril Tablets, USP, 25 mg Tablets, Packaged in A) 100 Count Bottles (NDC: 64679-0903-01) and B) 1000 Count Bottles (NDC: 64679-0903-02), Rx only. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA.

Quantity: A) 162,743 Bottles and B) 14,205 Bottles

Why Was This Recalled?

CGMP Deviations: Firm did not adequately investigate customer complaints.

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.

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