• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of October 17, 2012

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description Moexipril HCl Tablets 7.5mg, 100 tabs, Rx Only, Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0574-0110-01 ,
Recall Number D-007-2013
Classification Class II
Code Info 2012028142 exp. 1/2014
Product Distributed Qty 2267 bottles
Reason For Recall Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril HCl Tablets 7.5mg (expiration 1/2014) because of a non-conformity dissolution failure result found during routine stability testing at the 6 month test interval.

Event Detail

Event Id 63354
Product Type Drugs
Status Ongoing
Recalling Firm Paddock Laboratories, LLC
City Minneapolis
State MN
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-10-03
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide
-
-