JANUARY 2003

WEEK ENDING JANUARY 3

PRODUCT
Red Blood Cells, Leukoreduced, Recall # B-0314-3.
CODE
Units 107285050, 107301261, 107314546, 107307188.
RECALLING FIRM/MANUFACTURER
Blood Systems, Inc., Scottsdale, AZ, by telephone on May 30, 2002. Firm initiated recall is complete.
REASON
Blood products, which were below the firm's specification for product volume, were distributed.
VOLUME OF PRODUCT IN COMMERCE
4 units.
DISTRIBUTION AZ.

PRODUCT
Red Blood Cells, Leukoreduced, Recall # B-0316-3.
CODE
Units 107257323, 107268811(Split unit), 107251198.
RECALLING FIRM/MANUFACTURER
Blood Systems, Inc., Scottsdale, AZ, by telephone on May 31, 2002 and by letter dated June 25, 2002. Firm initiated recall is complete.
REASON
Blood products, which were below the firm's specification for product volume, were distributed.
VOLUME OF PRODUCT IN COMMERCE
4 units.
DISTRIBUTION
AZ.

PRODUCT
Red Blood Cells, Leukoreduced, Recall # B-0317-3.
CODE
Units 10727-4474, 10729-7670.
RECALLING FIRM/MANUFACTURER
Blood Systems, Inc., Scottsdale, AZ, by telephone on June 5, 2002 and by letter dated June 25, 2002. Firm initiated recall is complete.
REASON
Blood products, which were below the firm's specification for product volume, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
AZ.

PRODUCT
Red Blood Cells, Leukocytes Reduced, Recall # B-0318-3.
CODE
Unit number 53FE72562.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, Greater Chesapeake and Potomac Region, Baltimore, MD, by letters dated August 26, 2002 and September 26, 2002.
Firm initiated recall is complete.
REASON
Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
Washington DC

PRODUCT
a) Red Blood Cells, Leukocytes Reduced, Recall # B-0319-3;
b) Platelets, Recall # B-0320-3;
c) Fresh Frozen Plasma, Recall # B-0321-3.
CODE
a); b) and c) Unit number 53FN75872.

RECALLING FIRM/MANUFACTURER
The American National Red Cross, Greater Chesapeake and Potomac Region, Baltimore, MD, by letters dated April 26, 2002. Firm initiated recall is complete.
REASON
Blood products, that tested negative for hepatitis, but were collected from an ineligible donor due to a history of jaundice, were distributed.
VOLUME OF PRODUCT IN COMMERCE
3 units.
DISTRIBUTION
Washington DC and MD.

PRODUCT
Red Blood Cells, Leukocytes Reduced, Recall # B-0322-3;
CODE
Unit number 29KF16940;
RECALLING FIRM/MANUFACTURER
The American National Red Cross,Mid-Atlantic Region, Norfolk, VA, by letters and fax on April 12 and 22, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from a donor that did not answer one of the medical history questions concerning behavior known to increase risk of infection with the human immunodeficiency virus (HIV), were distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
NC and CA.

PRODUCT
a) Red Blood Cells, Leukoreduced, Recall # B-0326-3;
b) Recovered Plasma, Recall # B-0327-3.
CODE
a) and b) Unit 29FV51912.
RECALLING FIRM/MANUFACTURER
American Red Cross, Mid-Atlantic Region Blood Services, Norfolk, VA, by telephone on March 4, 2002 and by letter dated March 11, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from a donor whose health history screening was not adequately performed, were distributed
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
VA.

PRODUCT
Recovered Plasma, Recall # B-0328-3.
CODE
Units 53GR45262, 53GM31597.
RECALLING FIRM/MANUFACTURER
American Red Cross, Greater Chesapeake and Potomac Region, Baltimore, MD, by letter on July 18, 2002 and September 26, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from a donor who was at increased risk for new variant Creutzfeldt Jakob Disease (nvCJD), were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
CA.

PRODUCT
a) Red Blood Cells, Leukocytes Reduced, Recall # B-0329-3;
b) Platelets, Recall # B-0330-3.
CODE
a) Unit T91364;
b) Unit T91364 - pooled Platelet ID # - P13903.
RECALLING FIRM/MANUFACTURER
The Blood Center of Southeastern Wisconsin, Inc., Milwaukee, WI, by telephone and letter dated November 26, 2001. Firm initiated recall is complete.
REASON
Blood products, collected from a donor who reported travel to an area designated as endemic for malaria and being treated for pernicious anemia, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
WI.

PRODUCT
Red Blood Cells, Leukocytes Reduced, Recall # B-0342-3.
CODE
Unit number 33GE52670.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, Connecticut Region, Farmington, CT, by letter on October 3, 2002. Firm initiated recall is complete.
REASON
Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
CT.

PRODUCT
Platelets Pheresis, Leukocytes Reduced, Recall # B-0343-3.
CODE
Unit number 32KP25958 (distributed as two split products).
RECALLING FIRM/MANUFACTURER
The American National Red Cross, Badger-Hawkeye Region, Madison, WI, by letter on April 30, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from an unsuitable donor based on travel to an area considered endemic for malaria, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
IL.

PRODUCT
a) Red Blood Cells, Leukocytes Reduced, Recall # B-0344-3;
b) Platelets, Leukocytes Reduced, Recall # B-0345-3.
CODE
a) and b) Unit number 17KX83926.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, North Central Region, St. Paul, MN, by letter on April 30, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from an unsuitable donor based on travel to an area considered endemic for malaria, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
MN.

PRODUCT
Red Blood Cells, Leukocytes Reduced, Recall # B-0346-3.
CODE
Unit number 17KW43154.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, North Central Region, St. Paul, MN, by letter on February 26, 2002. Firm initiated recall is complete.
REASON
Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
CA.

PRODUCT
Red Blood Cells, Leukocytes Reduced, Recall # B-0347-3.
CODE
Unit number 17FZ53601.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, North Central Region, St. Paul, MN, by letter on February 15, 2002. Firm initiated recall is complete.
REASON
Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
MA.

PRODUCT
a) Red Blood Cells, Leukocytes Reduced, Recall # B-0348-3;
b) Recovered Plasma, Recall # B-0349-3.
CODE
a) and b) Unit number 17KV11561.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, North Central Region, St. Paul, MN, by letters on December 13 and 14, 2001. Firm initiated recall is complete.
REASON
Blood products, that tested negative for the antibody to hepatitis C virus (anti-HCV), but were collected from an ineligible donor based on the disclosure of a previous positive test for anti-HCV, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
MA and CA.

PRODUCT
Recovered Plasma, Recall # B-0323-3.
CODE
Unit number 29KF16940.
RECALLING FIRM/MANUFACTURER
The American National Red Cross,Mid-Atlantic Region, Norfolk, VA, by letters and fax on April 12 and 22, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from a donor that did not answer one of the medical history questions concerning behavior known to increase risk of infection with the human immunodeficiency virus (HIV), were distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
NC and CA.

PRODUCT
a) Cryoprecipitated AHF, Recall # B-0324-3;
b) Plasma, Recall # B-0325-3.
CODE
a) and b) Unit number 29KY11650.
RECALLING FIRM/MANUFACTURER
The American National Red Cross, Mid-Atlantic Region,Norfolk, VA, by telephone and letter July 8 and 15, 2002. Firm initiated recall is complete.
REASON
Blood products, collected from an ineligible donor due to use of the medication Sulfasalazine, were distributed.
VOLUME OF PRODUCT IN COMMERCE
2 units.
DISTRIBUTION
NC and NY.

PRODUCT
Recovered Plasma, Recall # B-0331-3.
CODE
Unit T91364.
RECALLING FIRM/MANUFACTURER
The Blood Center of Southeastern Wisconsin, Inc., Milwaukee, WI, by telephone and letter dated November 26, 2001. Firm initiated recall is complete
REASON
Blood products, collected from a donor who reported travel to an area designated as endemic for malaria and being treated for pernicious anemia, were distributed.
VOLUME OF PRODUCT IN COMMERCE
1 unit.
DISTRIBUTION
WI.

WEEK ENDING JANUARY 10

PRODUCT

Human tissue for transplantation of the following types from Donor ID #s

D0102466 and D0102484:

Recall # B-0300-3.

Cancellous Chips;Canc/cort dowel;Patellar Block;Graftech cervical spacer;Graftech cortical spacer ;Graftech cortical spacer-long;

Graftech posterior ramp;Graftech posterior ramp long;Femur head;Cort/canc dental powder;DBF Matrix.

CODE

Units D01024660021, D01024660022, D01024660023, D01024660024,

D01024660025, D01024660026, D01024840003,

D01024840004, D01024840005, D01024840006, D01024840007,

D01024840008;

Units D01024660017, D01024660018, D01024660019, D01024660020,

D01024660046

Units D01024660044, D01024660045;

Units D01024660029, D01024660030, D01024660031, D01024660032,

D01024660033, D01024660034, D01024660035, D01024660036, D01024660037,

D01024660038, D01024660039, D01024660040, D01024660041;

Units D01024660111, D01024660112, D01024660113, D01024660114,

D01024660115, D01024660116, D01024660117, D01024660118, D01024660119,

D01024660120, D01024660121, D01024660122, D01024660123, D01024660124,

D01024660125, D01024660126, D01024660127, D01024660128, D01024660129;

Units D01024660107, D01024660108, D01024660109, D01024660110;

Units D01024660078, D01024660079, D01024660080, D01024660081,

D01024660082, D01024660083, D01024660084, D01024660085, D01024660086,

D01024660087, D01024660088, D01024660089, D01024660090, D01024660091,

D01024660092, D01024660093, D01024660094, D01024660095, D01024660096,

D01024660097, D01024660098, D01024660099, D01024660100, D01024660101,

D01024660102, D01024660103, D01024660104, D01024660105, D01024660106;

Units D01024660074, D01024660075, D01024660076, D01024660077;

Units D01024660001, D01024660002;

Unit 01024660502;

Unit D01024840043.

RECALLING FIRM/MANUFACTURER

American Red Cross Tissue Services, Lorton, VA, by telephone on September

30, 2002 and by letter dated October 7, 2002. Firm initiated recall is

complete.

REASON

Human tissues for transplantation were distributed and were subsequently

reported to have tested repeatedly reactive for hepatitis B surface

antigen (HBsAg).

VOLUME OF PRODUCT IN COMMERCE

126 units.

DISTRIBUTION

Nationwide.

PRODUCT

a) Red Blood Cells, Leukoreduced, Recall # B-0351-3;

b) Red Blood Cells, Recall # B-0352-3.

CODE

a) Units LN51836, LN50030;

b) Unit FQ23844.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeastern Wisconsin, Inc., Milwaukee, WI, by

telephone on August 31, 2001 and by letter dated September 4, 2001. Firm

initiated recall is complete.

REASON

Blood products, collected from a donor who should have been deferred due

to use of the drug Cytotec, were distributed.

VOLUME OF PRODUCT IN COMMERCE

3 units.

DISTRIBUTION

WI.

PRODUCT

a) Red Blood Cells, Leukoreduced, Recall # B-0355-3;

b) Platelets, Recall # B-0356-3.

CODE

a) and b) Unit 32KN04017.

RECALLING FIRM/MANUFACTURER

American Red Cross Blood Services, Badger-Hawkeye Region, Madison, WI,

by letter dated April 19, 2002. Firm initiated recall is complete.

REASON

Blood products, collected from a donor who was at increased risk for new

variant Creutzfeldt Jakob Disease (nvCJD), were distributed.

VOLUME OF PRODUCT IN COMMERCE

2 units.

DISTRIBUTION

IL.

PRODUCT

Source Plasma, Recall # B-0365-3

CODE

98OWIA0594, 98OWIA1197, 98OWIA1814, 98OWIA2511, 98OWIA3161, 98OWIA3846,

98OWIA4447, 98OWIA5844, 98OWIA6621, 98OWIA7344, 98OWIA8105, 98OWIA8796,

98OWIA9532, 98OWIB0118, 98OWIB0754, 98OWIB1436, 98OWIB2328, 98OWIB3696,

98OWIB3783, 98OWIB6843, 98OWIB7678, 98OWIB8303, 98OWIC4340, 98OWIC5400,

98OWIC6657, 98OWIC7277, 98OWIC7854, 98OWIC9050, 98OWID1265, 98OWID1793,

98OWID2343, 98OWID2924, 98OWID3493, 98OWID4037, 98OWID4600, 98OWID5074,

98OWID5639, 98OWID6740, 98OWID7240, 98OWID7810, 98OWID8356, 98OWID8933,

98OWID9473, 98OWIE0058, 98OWIE1096, 98OWIE1681, 98OWIE2227, 98OWIE2843,

98OWIE3403, 98OWIE4018, 98OWIE4630, 98OWIE5276, 98OWIE5904, 98OWIE6495,

98OWIE7095, 98OWIF0287, 98OWIF0987, 98OWIF1658, 98OWIF2305, 98OWIF2993,

98OWIF3663, 98OWIF4422, 98OWIF6190, 98OWIF6949, 98OWIF9728,

98OWIG0134,99OWIA2983, 99OWIA3574, 99OWIA4152, 99OWIA4708, 99OWIA5277,

99OWIA7824, 99OWIA8489, 99OWIA9078, 99OWIA9741, 99OWIB0396, 99OWIB1767,

99OWIB2487, 99OWIB3024, 99OWIB3558, 99OWIB4229, 99OWIB4955, 99OWIB5634,

99OWIB7622, 99OWIB8274, 99OWIB8964, 99OWIB9608, 99OWIC0291, 99OWIC0942,

99OWIC1600, 99OWIC2221, 99OWIC3550, 99OWIC4134, 99OWIC4697, 99OWIC5287,

99OWIC5850, 99OWIC6375, 99OWIC7988, 99OWIC8517, 99OWIC9085, 99OWIC9654,

99OWID0224, 99OWID0786, 99OWID1391, 99OWID1977, 99OWID2447, 99OWID3022,

99OWID3733, 99OWID4453, 99OWID5090, 99OWID5838, 99OWID6480, 99OWID7206,

99OWID7830, 99OWID8580, 99OWID9209, 99OWID9963, 99OWIE0581, 99OWIE1333,

99OWIE1960, 99OWIE2740,99OWIE3373, 99OWIE4074, 99OWIE4715, 99OWIE5483,

99OWIE6116, 99OWIE6852, 99OWIE7473, 99OWIE8203, 99OWIE8848, 99OWIE9578,

99OWIF0190, 00OWID0680, 00OWID1253, 00OWID2396, 00OWID2942, 00OWID3539,

00OWID4112, 00OWID4698, 00OWID5218, 00OWID5788, 00OWID6301.

RECALLING FIRM/MANUFACTURER

Recalling Firm: Community Bio-Resources, Inc., Hoover, AL, by fax dated

November 30, 2000.

Manufacturer: Community Bio-Resources, Inc., Oshkosh, WI. Firm

initiated recall is complete.

REASON

Blood products, collected from a donor whose health history screening was

inadequately performed, were distributed

VOLUME OF PRODUCT IN COMMERCE

140 units.

DISTRIBUTION

MI and Austria.

PRODUCT

Source Plasma, Recall # B-0368-3.

CODE

Units 00OWIC0289, 00OWIC0251, 00OWIC1554, 00OWIC1981,

00OWIC3195, 00OWIC4571, 00OWIC5739, 00OWIC6872, 00OWID3484.

RECALLING FIRM/MANUFACTURER

Recalling Firm: Community Bio-Resources, Inc., Hoover, AL, by fax dated July 26, 2000 or August 28, 2000.

Manufacturer: Community Bio-Resources, Inc., Oshkosh, WI. Firm initiated

recall is complete.

REASON

Blood products, collected from a donor who had not completed the

CJD/nvCJD increased risk questions, were distributed.

VOLUME OF PRODUCT IN COMMERCE

9 units.

DISTRIBUTION

MI and Austria.

PRODUCT

Source Plasma, Recall # B-0369-3.

CODE

Unit 00GWIC4894.

RECALLING FIRM/MANUFACTURER

Recalling Firm: Community Bio-Resources, Inc., Hoover, AL, by letter

dated July 25, 2000.

Manufacturer: Community Bio-Resources, Inc., Green Bay, WI. Firm

initiated recall is complete.

REASON

Blood product, collected from a donor who had not completed the CJD/nvCJD

increased risk questions, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

Austria.

PRODUCT

Source Plasma, Recall # B-0370-3

CODE

Unit 00MWIC9431

RECALLING FIRM/MANUFACTURER

Recalling Firm: Community Bio-Resources, Inc., Hoover, AL, by letter

dated July 31, 2000.

Manufacturer: Community Bio-Resources, Inc., Menasha, WI. Firm initiated

recall is complete.

REASON

Blood product, collected from a donor who had not completed the CJD/nvCJD

increased risk questions, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

Austria.

PRODUCT

Platelets Pheresis, Leukocytes Reduced Irradiated, Recall # B-0372-3

CODE

Unit number 0870914.

RECALLING FIRM/MANUFACTURER

Memorial Blood Centers of Minnesota, Minneapolis, MN, by telephone on

September 17, 2001. Firm initiated recall is complete.

REASON

Blood product, labeled with the incorrect expiration date, was

distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

MN.

PRODUCT

a) Red Blood Cells, Leukocytes Reduced, Recall # B-0373-3;

b) Cryoprecipitated AHF, Pooled, Recall # B-0374-3;

c) Recovered Plasma, Recall # B-0375-3.

CODE

a) and c) Unit number FQ32630;

b) Pool number P27248.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeast Wisconsin, Inc., Milwaukee, WI, by

telephone on March 22, 2002 and by letters on March 26, 2002. Firm

initiated recall is complete.

REASON

Blood products, that tested negative for hepatitis B surface antigen

(HBsAg), but were collected from an ineligible donor based on the

disclosure of a previous positive test for HBsAg, were distributed.

VOLUME OF PRODUCT IN COMMERCE

3 units.

DISTRIBUTION

WI and Switzerland.

PRODUCT

Red Blood Cells, Leukocytes Reduced, Recall # B-0376-3.

CODE

Unit number FQ31716.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeast Wisconsin, Inc., Milwaukee, WI, by

telephone on July 10, 2002 and by letter dated July 25, 2002. Firm

initiated recall is complete.

REASON

Blood product, collected from an unsuitable donor based on living in an

area considered endemic for malaria, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

WI.

PRODUCT

Whole Blood, Leukocytes Reduced, Recall # B-0377-3

CODE

Unit number FW43708.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeast Wisconsin, Inc., Milwaukee, WI, by

telephone on August 19, 2002. Firm initiated recall is complete.

REASON

Blood product, collected from an unsuitable donor based on travel to an

area considered endemic for malaria, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

WI.

PRODUCT

Red Blood Cells, Leukocytes Reduced, Recall # B-0378-3.

CODE

Unit number R17684.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeast Wisconsin, Inc., Milwaukee, WI, by letter

dated August 29, 2002 and by telephone on August 30, 2002. Firm initiated

recall is complete.

REASON

Blood product, collected from an unsuitable donor based on travel to an

area considered endemic for malaria, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

WI.

PRODUCT

Red Blood Cells, Recall # B-0379-3.

CODE

Unit number R16143.

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeast Wisconsin, Inc., Milwaukee, WI, by letter

dated April 11, 2002 and by telephone on April 16, 2002. Firm initiated

recall is complete.

REASON

Blood product, collected from a donor who should have been deferred due

to use of the medication Valtrex, was distributed.

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

VA.

PRODUCT

Source Plasma, Recall # B-0311-3.

CODE

Units 54DPCGHT, 54DPCMLT, 54DPBYSF.

RECALLING FIRM/MANUFACTURER

Aventis Bio-Services, Inc., Milwaukee, WI, by letter dated March 12,

2002. Firm initiated recall is complete.

REASON

Blood products, collected from a donor whose arm inspection was not

documented, were distributed.

VOLUME OF PRODUCT IN COMMERCE

3 units.

DISTRIBUTION

IL.

PRODUCT

Recovered Plasma, Recall # B-0353-3.

CODE

Units LN51836, LN50030, FQ23844

RECALLING FIRM/MANUFACTURER

The Blood Center of Southeastern Wisconsin, Inc., Milwaukee, WI, by

telephone on August 31, 2001 and by letter dated September 4, 2001. Firm

initiated recall is complete.

REASON

Blood products, collected from a donor who should have been deferred due

to use of the drug Cytotec, were distributed.

VOLUME OF PRODUCT IN COMMERCE

3 units.

DISTRIBUTION

WI.

PRODUCT

Platelet, Pheresis, Leukoreduced, Irradiated. Recall # B-0354-3.

CODE

Units 32FP11122, 32GP19286.

RECALLING FIRM/MANUFACTURER

American Red Cross Blood Services,Badger-Hawkeye Region, Madison, WI, by

letter dated April 10, 2002. Firm initiated recall is complete.

REASON

Blood products that were out of controlled storage for more than thirty

minutes were distributed.

VOLUME OF PRODUCT IN COMMERCE

2 units.

DISTRIBUTION

MI.

PRODUCT

Source Plasma, Recall # B-0357-3.

CODE

Units 54DPBJZH, 54DPVSS, 54DPDWZS, 54DPCRJJ

RECALLING FIRM/MANUFACTURER

Aventis Bio-Services, Inc., Milwaukee, WI, by letter dated April 12,

2002. Firm initiated recall is complete.

REASON

Blood products, collected from a donor whose arm inspection was not

documented, were distributed.

VOLUME OF PRODUCT IN COMMERCE

4 units.

DISTRIBUTION

IL.

PRODUCT

Source Plasma, Recall # B-0358-3.

CODE

Unit 54DPCWRQ

RECALLING FIRM/MANUFACTURER

Aventis Bio-Services, Inc., Milwaukee, WI, by letter dated April 12,

2002. Firm initiated recall is complete.

REASON

Blood product, which was collected from a donor with an elevated body

temperature, was distributed

VOLUME OF PRODUCT IN COMMERCE

1 unit.

DISTRIBUTION

IL.

PRODUCT

Platelets, Irradiated, Recall # B-0371-3.

CODE

Unit S09603.

RECALLING FIRM/MANUFACTURER

Virginia Blood Services, Richmond, VA, by letter dated September 3, 2002.