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From: TSS ()
Subject: Re: New case (3rd) of variant CJD associated with blood transfusion
Date: February 9, 2006 at 6:52 am PST

In Reply to: New case (3rd) of variant CJD associated with blood transfusion posted by TSS on February 9, 2006 at 6:22 am:

PRODUCT
Source Plasma, Recall # B-0584-6
CODE
Units VL53767, ZZ031076, ZZ030881, ZZ03046, VL151413, VL151144, VL50837
RECALLING FIRM/MANUFACTURER
BioLife Plasma Services LP, Shreveport, LA, by facsimile dated October 6, 2003. Firm initiated recall is complete.
REASON
Source Plasma, collected from a donor who was at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.
VOLUME OF PRODUCT IN COMMERCE
7 units
DISTRIBUTION
NC

END OF ENFORCEMENT REPORT FOR FEBRUARY 1, 2006

###

http://www.fda.gov/bbs/topics/enforce/2006/ENF00937.html

PRODUCT
Red Blood Cells, Recall # B-0552-6
CODE
Unit number: 4426304
RECALLING FIRM/MANUFACTURER
Florida's Blood Center, Inc., St. Petersburg, FL, by facsimile on July 8, 2005. Firm initiated recall is complete.
REASON
Blood product, collected from a donor who may have been at increased risk for new variant Creutzfeldt-Jakob Disease (nvCJD), was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit
DISTRIBUTION
FL

END OF ENFORCEMENT REPORT FOR JANUARY 25, 2006

###

http://www.fda.gov/bbs/topics/enforce/2006/ENF00936.html

===================================



PRODUCT
a) Red Blood Cells, Leukocytes
Reduced, Recall # B-0492-6;
b) Recovered Plasma, Recall # B-0497-6
CODE
a) and b) Unit number: 4101212
RECALLING FIRM/MANUFACTURER
Northwest Florida Blood Center, Inc., Pensacola, FL, by telephone and facsimile on March 7, 2003. Firm initiated recall is complete.
REASON
Blood products, collected from an unsuitable donor due to a history of travel to an area considered at increased risk of exposure to variant Creutzfeldt-Jakob Disease (nvCJD), were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units
DISTRIBUTION
FL

_______________________________

END OF ENFORCEMENT REPORT FOR JANUARY 18, 2006

###

http://www.fda.gov/bbs/topics/enforce/2006/ENF00935.html

PRODUCT
Source Plasma, Recall # B-0391-6
CODE
Unit number: 7030260750
RECALLING FIRM/MANUFACTURER
ZLB Bioplasma, Inc., San Antonio, TX, by facsimile and telephone on September 29, 2003. Firm initiated recall is complete.
REASON
Blood product, which was collected from a donor who was deferred due to risk factors associated with variant Creutzfeldt-Jakob disease (vCJD) travel, was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit
DISTRIBUTION
FL

_______________________________

PRODUCT
a) Red Blood Cells, Leukocytes Reduced
Recall # B-0456-6;
b) Recovered Plasma, Recall # B-0457-6
CODE
a) Unit number: 06FR39967;
b) Unit numbers: 06FR37676, 06FR39967
RECALLING FIRM/MANUFACTURER
American National Red Cross, Southern California Region, Pomona, California, by telephone on June 2, 2002, and by letter dated, June 20, 2002, and by facsimile transmission dated June 19, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from a donor who was at increased risk of variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
VOLUME OF PRODUCT IN COMMERCE
3 units
DISTRIBUTION
CA and Switzerland

_______________________________

END OF ENFORCEMENT REPORT FOR JANUARY 4, 2006

###

http://www.fda.gov/bbs/topics/enforce/2006/ENF00933.html

TSS




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