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SafetyAlerts
August 27, 2003

Recall Update: Schweppes Ginger Ale Recall is Complete

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

PRODUCT
Schweppes Ginger Ale 8 pack cases of 2 liter bottles. Recall # F-471-3.

CODE
FEB 1003 XXXXZG110622 where XXXX indicates the military time that the product was produced from 1500-1630.

RECALLING FIRM/MANUFACTURER
Dr Pepper Seven Up, Inc., Plano, TX, via memo on November 20, 2002. Firm initiated recall is complete.

REASON
The product contained undeclared quinine.

VOLUME OF PRODUCT IN COMMERCE
1,374 cases of 8 bottles each.

DISTRIBUTION
MO and IL
.

 
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Health Professional:

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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.