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SafetyAlerts
November 12,  2003

Bayer Corporation Has Recalled TRASYLOL Injection

(SafetyAlerts) - The FDA has released the following information.

PRODUCT
TRASYLOL Injection (aprotinin), 200mL vial, Rx only. Recall # D-049-4.

CODE
Batch Number: 250076L Expiration Date: 2/2004.

RECALLING FIRM/MANUFACTURER
Bayer Corporation, West Haven, CT, by letter dated October 6, 2003. Firm initiated recall is ongoing.

REASON
Particulates: Delayed formation of a precipitate (stability).

VOLUME OF PRODUCT IN COMMERCE
2,649 vials.

DISTRIBUTION
Nationwide
.

 
Selected Recent Recalls


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During 2000 there were over
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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.