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Posted August 09, 2002

Recall of 7 Herbal Products from Botanic Lab in US and Abroad

The U.S. Food and Drug Administration (FDA) released the following Class II recall information in its August 7, 2002 Enforcement Report. A Class II recall is a situation in which use or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where probability of seroius adverse health consequences is remote. This recall relates to a similar warning issued by Health Canada in June (see June 21 posting in the Recalls and Warnings archive):

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