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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K972435
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ULTIMA*LX STM,POL 10/12TAP/SZ1 Packaging: The product was packaged within inner and outer PETG bl... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/SZ2 Packaging: The product was packaged within inner and outer PETG bl... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/SZ3 Packaging: The product was packaged within inner and outer PETG bl... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/SZ4 Packaging: The product was packaged within inner and outer PETG bl... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/4M Packaging: The product was packaged within inner and outer PETG bli... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/1M Packaging: The product was packaged within inner and outer PETG bli... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/2M Packaging: The product was packaged within inner and outer PETG bli... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/3M Packaging: The product was packaged within inner and outer PETG bli... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/SZ5 Packaging: The product was packaged within inner and outer PETG bl... 2 06/29/2012 DePuy Orthopaedics, Inc.
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