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

Enforcement Report - Week of October 3, 2012

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description Synthroid (levothyroxine sodium) Tablets USP, 75 mcg, Rx Only, 90-Count Bottle, Abbott Laboratories, North Chicago, IL 60064, NDC: 0074-5182-90.
Recall Number D-1695-2012
Classification Class II
Code Info Lot: 18353A8, Exp 08/31/2013
Product Distributed Qty 42,596 Bottles
Reason For Recall Defective Container: A number of Synthroid bottles have a localized thin wall defect on the bottom which may potentially impact the stability of the tablets.

Event Detail

Event Id 62674
Product Type Drugs
Status Ongoing
Recalling Firm Abbott Laboratories
City Abbott Park
State IL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-07-19
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide
-
-