July 2015 FDA Recall Drug by Vintage Pharmaceuticals Llc Dba Qualitest Pharmaceuticals
D-1406-2015 - Failed Dissolution Specifications
This Class II drug recall was voluntarily initiated by Vintage Pharmaceuticals Llc Dba Qualitest Pharmaceuticals on July 29, 2015 for the product Drug. The FDA reported the reason for recall as failed dissolution specifications. The product was distributed Nationwide and the recall is currently terminated.
Recall Number: D-1406-2015
Failed Dissolution Specifications
07-29-2015
09-09-2015
8,705 bottles
Recall Profile & Regulatory Data
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
The firm responsible for the recall.
Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Nationwide and Puerto Rico
03-29-2016
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
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
Batch or Lot Expiration Information
Lot# a) C0570215B; Exp 02/17 b) C0570215A; Exp 02/17
