Class III — Low Risk

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

Mavik¿ trandolapril tablets 4mg Recalled by AbbVie Inc. Due to Labeling: Incorrect Package Insert; product packaged with outdated...

Date: August 1, 2013
Company: AbbVie 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 AbbVie Inc. directly.

Affected Products

Mavik¿ trandolapril tablets 4mg, 100 count bottle, Rx only, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ for Abbott Laboratories, North Chicago, IL 60064, USA

Quantity: 704 bottles

Why Was This Recalled?

Labeling: Incorrect Package Insert; product packaged with outdated version of the insert

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About AbbVie Inc.

AbbVie Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

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