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Administration (FDA) Issues Urgent Recall Of Injectable Drugs T he Food and Drug Administration (FDA) on January 25, 2001, issued an urgent recall of 38 injectable drugs marketed by Phyne Pharmaceuticals of Scottsdale, Arizona. Another company, AMRAM Incorporated, of Rathdrum, Idaho, manufactured these products for Phyne, which was AMRAM s sole customer. Last December 14, AMRAM notified Phyne that it was recalling these products because they were manufactured under substandard conditions. Th.

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