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SafetyAlerts
June 6, 2002
Updated June 28, 2002

Pharmacia (Perth) Has Recalled Doxorubicin Hydrochloride Injection

The FDA has updated the following information found in red.

Irvine, CA (SafetyAlerts) - The Food and Drug Administration (FDA) said Pharmacia (Perth) has recalled Doxorubicin Hydrochloride Injection.

P
RODUCT
Doxorubicin Hydrochloride Injection, USP, 50mg/25mL (2mg/mL), 25mL Single Dose Vial, Rx only. Recall # D-281-2.

CODE
Lot T049 Exp. 9/2002.

RECALLING FIRM/MANUFACTURER
Pharmacia (Perth) Pty. Limited, Bentley WA 6102 Australia. Firm initiated recall is ongoing.

REASON
Lack of assurance of sterility.

VOLUME OF PRODUCT IN COMMERCE
20,520 vials.

DISTRIBUTION
Nationwide.

 
Selected Recent Recalls


Health Professional:

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During 2000 there were over
1050 products recalled in the United
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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.