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SafetyAlerts
July 25, 2000

Bulk Botanical Dietary Supplement Recalled by Eudaemonic Corporation

Omaha, NE (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Eudaemonic Corporation is conducting a recall of Astragulus Capsules because the product was contaminated with Salmonella.

PRODUCT
Astragulus Capsules, 500 mg, in bulk containers of 10,000 capsules, a botanical dietary supplement.

Recall #F-620-0.  Class I

CODE
Lot #21592.

MANUFACTURER
ABS Corporation, doing business as Eudaemonic Corporation, Omaha, Nebraska.

RECALLED BY
Manufacturer, by telephone on September 2, 1999. Firm-initiated recall complete.   This is the first public notice issued by the FDA.

DISTRIBUTION
North Dakota.

QUANTITY
235,872 capsules were distributed.

Questions concerning this recall may be directed to the FDA at 1-888-INFO-FDA.

Notice of this product warning was sent via email to SafeMail subscribers July 25, 2000.

 
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Health Professional:

Did you know?
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.