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

Enforcement Report - Week of July 24, 2013

  • Print
  • Share
  • E-mail

Product Detail

Product Description Plasma Frozen Within 24 Hours After Phlebotomy (FP24)
Recall Number B-1825-13
Classification Class II
Code Info W045008120117; W045008117439; W045008117425; W045008119923; W045008119929; W045008111075; W045008120118; W045008117428; W045008913211; W045008115790; W045008111068; W045008110803; W045008095756; W045008111946; W045008108338; W045008108721; W045008119951; W045008119995; W045008119926; W045008108796; W045008120116; W045008129855; W045008129852; W045008120025; W045008119991; W045008119893; W045008117463; W045008115778; W045008115702; W045008115633; W045008111976
Product Distributed Qty 31 Units
Reason For Recall Blood products, collected in a manner that may have compromised the sterility of the units, were distributed.

Event Detail

Event Id 53621
Product Type Biologics
Status Terminated
Recalling Firm Community Blood Center Of Gtr KC
City Kansas City
State MO
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-02-03
Initial Firm Notification of Consignee or Public FAX
Distribution Pattern MO; KS; LA; CA;