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

Enforcement Report - Week of May 1, 2013

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description Source Plasma
Recall Number B-1064-13
Classification Class III
Code Info 5200026069, 5200026406, 5200027561, 5200027908, 5200028505, 5200028965, 5200029669, 5200030096, 5200030750, 5200034043, 5200034835, 5200035230, 5200035752, 5200036034, 5200036604, 5200036928, 5200037499, 5200037813, 5200038699, 5200039079, 5200039639
Product Distributed Qty 21 units
Reason For Recall Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed.

Event Detail

Event Id 59516
Product Type Biologics
Status Terminated
Recalling Firm Octapharma Plasma, Inc.
City Fort Worth
State TX
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2011-07-06
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern CA, Switzerland
-
-