US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 1, 2013 (13 years ago)

Mavik¿ trandolapril tablets 4mg, 100 count bottle, Rx only, Manufactured by Halo…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Labeling: Incorrect Package Insert; product packaged with outdated version of the insert

What was recalled

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

Recalling firm
AbbVie Inc.
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-901-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.