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

Enforcement Report - Week of December 11, 2013

  • Print
  • Share
  • E-mail

Event Detail

Event ID 66460
Product Type Veterinary
Status Ongoing
Recalling Firm Lloyd Inc. of Iowa
City Shenandoah
State IA
Country US
Voluntary/Mandated Voluntary: Firm Initiated
Recall Initiation Date 2013-10-03
Initial Firm Notification of
Consignee or Public
Distribution Pattern Distribution was made in the US to AL, AZ, CA, CO, FL, GA, HI ,IA, ID, IN KS, MI, MN, MO, MS, NC, NY, PA, TX, VA, WA and WI. No foreign distribution was made.

Product Detail

Product Description Code Info Classification Reason for Recall Product Quantity Recall Number
Lloyd Butorphic Injection, Butorphanol Tartrate, 10 mg/mL, 20 mL, C 4, ANDA 200-332. Manufactured by Akorn, Inc., Decatur, IL for Lloyd, Shenandoah, IA. Lot LA28410A and Lot LA29810A Class III The product is being recalled because of an incorrect expiration date listed on the product label. 4,466 vials V-010-2014