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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K083746
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FDA Recall
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Orasure QuickFlu Rapid A+B Test Manufactured for OraSure Technologies, Inc Bethlehem, PA 18015 USA.... 2 08/31/2012 Princeton Biomeditech Corp
Poly stat Flu A & B Test Manufactured for Polymedco 510 Furnace Dock Road Cortlandt Manor, NY ... 2 08/31/2012 Princeton Biomeditech Corp
Status Flu A + B Test Manufactured by Princeton Bio Meditech Corporation Monmouth Junction, NJ 0... 2 08/31/2012 Princeton Biomeditech Corp
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