PlainRecalls
FDA Drug Moderate Class II Terminated

Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811

Reported: September 9, 2015 Initiated: July 29, 2015 #D-1406-2015

Product Description

Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811

Reason for Recall

Failed Dissolution Specifications

Details

Units Affected
8,705 bottles
Distribution
Nationwide and Puerto Rico
Location
Huntsville, AL

Frequently Asked Questions

What product was recalled?
Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811. Recalled by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals. Units affected: 8,705 bottles.
Why was this product recalled?
Failed Dissolution Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on September 9, 2015. Severity: Moderate. Recall number: D-1406-2015.