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SafetyAlerts
August 27, 2003

Recall Update: New Diet Sunkist Orange Recall is Complete

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

PRODUCT
New Diet Sunkist Orange. Recall # F-466-3.

CODE
985067006 (Bottled October 14, 2002);
985070140 (Bottled October 21, 2002).

RECALLING FIRM/MANUFACTURER
Dr Pepper Seven Up, Inc., Plano, TX, by visit beginning November 1, 2002. Firm initiated recall is complete.

REASON
The product contained undeclared sweetening agent - acesulfame potassium.

VOLUME OF PRODUCT IN COMMERCE
1,200 cases.

DISTRIBUTION
TX
.

 
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.