COPD International   Your Support Network

You can learn to control this disease instead of letting it control you!

 

Return To The Main Library         <<<<>>>>         Return To The HomePage

 
 

SafetyAlerts
June 4, 2003


Purdue Frederick Company Has Recalled Senokot Granules

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

PRODUCT
Senokot Granules (standardized senna concentrate), Natural Vegetable Laxative, 15mg sennosides in each teaspoon, 6 oz and 12 oz bottles. Recall # D-262-3.

CODE
Lot No. RR61 exp. 10/2007; RA02 exp. 10/2007; RA11 exp. 10/2007.

RECALLING FIRM/MANUFACTURER
The Purdue Frederick Company, Stamford, CT, by telephone on April 15, 2003, and by letters on April 25, 2003. Firm initiated recall is ongoing.

REASON
Mold contamination-Inactive ingredient-Malt syrup lot used in granule manufacturing had expired and was later found to contain surface mold.

VOLUME OF PRODUCT IN COMMERCE
4,296 - 6oz. bottles; 2,419 - 12 oz. bottles.

DISTRIBUTION
Nationwide.

Send mail to: Webmaster@COPD-International.com with questions
or comments about this web site.
Copyright © 2002-2004 ----- COPD-International.com
Last modified:
June 6, 2003
Disclaimer