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SafetyAlerts
July 9, 2003

Meridian Pharmaceuticals Has Recalled Budesonide BP Micronized

(SafetyAlerts) - The Food and Drug Administration (FDA) released the following information.

PRODUCT
Budesonide BP Micronized, 500mg, 5g, 1g, 25g, 100g bottles, Caution: For manufacturing, processing and repackaging. Recall # D-274-3.

CODE
Lot numbers: 03100205, 03100206, 03100207, 03100208, 03100209, and 03200307.

RECALLING FIRM/MANUFACTURER
Meridian Pharmaceuticals, Inc., Decatur, AL, by letters on June 4, 2003. Firm initiated recall is ongoing.

REASON
Subpotent.

VOLUME OF PRODUCT IN COMMERCE
276 grams.

DISTRIBUTION
Nationwide
.

 
Selected Recent Recalls


Health Professional:

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During 2000 there were over
1050 products recalled in the United
States for safety reasons!

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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.