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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K071417
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System wh... 1 02/15/2013 DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System wh... 1 02/15/2013 DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System wh... 1 02/15/2013 DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System wh... 1 02/15/2013 DePuy Orthopaedics, Inc.
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